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      • witney, south east
      • contract
      • randstad business support
      JOB ROLE: Technologist LOCATION: Witney, Oxfordshire - please note we will not be accepting CVs from un-commutable locations.TYPE: ContractPAY RATE: Market rate Are you an enthusiastic Science Graduate who is interested in gaining experience with a well renowned Pharmaceutical company? If you have studied in the fields of Chemistry, Biomedical Science, Engineering or any related discipline, this could be the job for you! This is an office-based role with opportunity to be involved in the analysis of innovative medical devices. Randstad is recruiting a number of Technologists on behalf of a global medical device and pharmaceutical leader, who are dedicated to helping people reach their full health potential. The successful candidate will carry out technical activities as directed, in order to ensure that projects and investigations supporting the Manufacturing Unit, Materials Analysis, Laboratory and Product Test Operations are executed to plan. Training and support will be provided. In the absence of work experience, you must have a related qualification and a genuine interest in the subject matter. Ideal Experience/Qualifications:Qualification in a Science related subject area.Strong IT skills, especially Excel.Strong written and communication skillsAble to analyse and utilise data.Comfortable in presenting information and writing reports.Any work experience in this area is beneficial but not essential.A genuine interest to learn and a passion for the work involved.Are you a self starter interested in working for a company who makes a genuine difference to people's lives? Apply today to hear more about this great opportunity!Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      JOB ROLE: Technologist LOCATION: Witney, Oxfordshire - please note we will not be accepting CVs from un-commutable locations.TYPE: ContractPAY RATE: Market rate Are you an enthusiastic Science Graduate who is interested in gaining experience with a well renowned Pharmaceutical company? If you have studied in the fields of Chemistry, Biomedical Science, Engineering or any related discipline, this could be the job for you! This is an office-based role with opportunity to be involved in the analysis of innovative medical devices. Randstad is recruiting a number of Technologists on behalf of a global medical device and pharmaceutical leader, who are dedicated to helping people reach their full health potential. The successful candidate will carry out technical activities as directed, in order to ensure that projects and investigations supporting the Manufacturing Unit, Materials Analysis, Laboratory and Product Test Operations are executed to plan. Training and support will be provided. In the absence of work experience, you must have a related qualification and a genuine interest in the subject matter. Ideal Experience/Qualifications:Qualification in a Science related subject area.Strong IT skills, especially Excel.Strong written and communication skillsAble to analyse and utilise data.Comfortable in presenting information and writing reports.Any work experience in this area is beneficial but not essential.A genuine interest to learn and a passion for the work involved.Are you a self starter interested in working for a company who makes a genuine difference to people's lives? Apply today to hear more about this great opportunity!Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • sittingbourne, south east
      • temporary
      • £9.25 per hour
      • randstad inhouse services
      Are you looking for a new role, within an established company? Do you enjoy working with mechanics in a personal or work capacity? Then we may just have the role for you!Randstad are currently recruiting for a Service Centre Repair Technician for a well-known medical device company. Benefits you'll Love:Training and full personal protective equipment providedFree on-site parking Subsidised onsite canteen Outside seating areas Hours and Pay rate:£9.25 per hourMonday - Friday: 06:00am - 14:00pm and 14:00pm - 22:00pm37.5 hours This role is a 12 month ongoing contract Your Responsibilities:Diagnosing and repairing medical equipment Service, repair, and test Nutritional DevicesCarry out investigations of Nutritional DevicesMaintain records both soft and hard copyAssist in the maintenance and operation of the flow and tracking of devicesIdentify improvements Requirements:Mechanical experience, either in a work or personal capacityBasic IT skillsEligible to live and work in the UK With full training provided, what are you waiting for, click apply today!
      Are you looking for a new role, within an established company? Do you enjoy working with mechanics in a personal or work capacity? Then we may just have the role for you!Randstad are currently recruiting for a Service Centre Repair Technician for a well-known medical device company. Benefits you'll Love:Training and full personal protective equipment providedFree on-site parking Subsidised onsite canteen Outside seating areas Hours and Pay rate:£9.25 per hourMonday - Friday: 06:00am - 14:00pm and 14:00pm - 22:00pm37.5 hours This role is a 12 month ongoing contract Your Responsibilities:Diagnosing and repairing medical equipment Service, repair, and test Nutritional DevicesCarry out investigations of Nutritional DevicesMaintain records both soft and hard copyAssist in the maintenance and operation of the flow and tracking of devicesIdentify improvements Requirements:Mechanical experience, either in a work or personal capacityBasic IT skillsEligible to live and work in the UK With full training provided, what are you waiting for, click apply today!
      • witney, south east
      • contract
      • £40.00 - £55.00, per hour, Depending on experience
      • randstad cpe
      As CRA, you will:Conduct site visits and study monitoring to ensure all clinical studies meet procedural and GCP requirements.Prepare monitoring reports, study documentation/ files.Support conduct of site initiation visits.Support all aspects of study delivery at a site-levelTo Be considered for the role of CRA, you will:Educated to degree level in a relevant scientific fieldSite Monitoring experienceUnderstand diabetes and its treatment, understand technical aspects of the products Deliver studies according to Good Clinical Practice (GCP)Ideal experience : of working with medical devices and European and US regulations/standards affecting clinical investigations, in vitro diagnostic devices, medical devices and biologics (e.g. GCP, ISO15197, ISO14155) is desirableThis is a 12 Month contract based Witney, Oxfordshire. PAYE. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      As CRA, you will:Conduct site visits and study monitoring to ensure all clinical studies meet procedural and GCP requirements.Prepare monitoring reports, study documentation/ files.Support conduct of site initiation visits.Support all aspects of study delivery at a site-levelTo Be considered for the role of CRA, you will:Educated to degree level in a relevant scientific fieldSite Monitoring experienceUnderstand diabetes and its treatment, understand technical aspects of the products Deliver studies according to Good Clinical Practice (GCP)Ideal experience : of working with medical devices and European and US regulations/standards affecting clinical investigations, in vitro diagnostic devices, medical devices and biologics (e.g. GCP, ISO15197, ISO14155) is desirableThis is a 12 Month contract based Witney, Oxfordshire. PAYE. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • witney, south east
      • contract
      • £11.00 - £11.80 per hour
      • randstad cpe
      R&D Sensor Laboratory Technician to join a well-known healthcare company at their facility in Witney on a 12month contract. You will be responsible for the support of processes within the R&D Sensor Laboratories ensuring that all equipment and materials are available. You will be involved in the scheduling, building and testing of experimental sensor lots and to assist Scientists and Engineers in product development activities. The role will be involved with the planning and logistics of all R&D sensor-based studies including the production and support of tests, protocols and procedures.A secondary education in Science, English and Maths (or equivalent)Good written and oral skills are required to help with the completion of experimental test protocols, batch records and discussion of test resultsPrevious Laboratory or Manufacturing experience would be of benefit Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      R&D Sensor Laboratory Technician to join a well-known healthcare company at their facility in Witney on a 12month contract. You will be responsible for the support of processes within the R&D Sensor Laboratories ensuring that all equipment and materials are available. You will be involved in the scheduling, building and testing of experimental sensor lots and to assist Scientists and Engineers in product development activities. The role will be involved with the planning and logistics of all R&D sensor-based studies including the production and support of tests, protocols and procedures.A secondary education in Science, English and Maths (or equivalent)Good written and oral skills are required to help with the completion of experimental test protocols, batch records and discussion of test resultsPrevious Laboratory or Manufacturing experience would be of benefit Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • witney, south east
      • contract
      • £11.50 per hour
      • randstad cpe
      My client, a leading manufacturer in the healthcare devices, has a requirement for a QA Associate to join their team in Witney on a 3 month contract. As QA Associate, you will:Support the activities to review batch records, compile the Device History Record and approval of in-process product and finished goods for all product lines.Inspect and release of label copy, including the mastering on new label copy.MACPAC Transactions filings and records To be considered for for the role of QA Associate, you will:Secondary level English and Maths Strong attention to detail Commutable to Witney on a daily basisThis is a 3 month PAYE contract with the possibility of ongoing extension. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      My client, a leading manufacturer in the healthcare devices, has a requirement for a QA Associate to join their team in Witney on a 3 month contract. As QA Associate, you will:Support the activities to review batch records, compile the Device History Record and approval of in-process product and finished goods for all product lines.Inspect and release of label copy, including the mastering on new label copy.MACPAC Transactions filings and records To be considered for for the role of QA Associate, you will:Secondary level English and Maths Strong attention to detail Commutable to Witney on a daily basisThis is a 3 month PAYE contract with the possibility of ongoing extension. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • witney, south east
      • contract
      • £11.50 per hour
      • randstad cpe
      Do you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual and as part of a team? We are looking for a Product Test Technician to join a global medical device and healthcare leader based in Witney.This is a 12-month contract with the potential for extension, working 37.5 hours per week, 07:00 - 15:00. The successful candidate will be handling, sampling and testing the finished product. Benefits:Friendly and welcoming teamFree onsite parkingOnsite canteenOutside seating areasWeekly onsite Covid testing available for staffResponsibilities:Perform the set-up, sampling and testing of finished products.Support development/validation trialsSupport product performance monitoring Make sure activities are completed as scheduled on time and in full to meet business and customer's needsAccurate recording and review of data of finished productsPro-actively supporting new/changed procedures, processes, and products within the area, including associated validation/verification activitiesSupporting the design, planning, and delivery of new training materials and the review, evaluation, and delivery of existing training materialsQualifications:Secondary level education including English and MathsRequirements:Good written and oral skills are required to help generate clear and legible documentation and understand technical informationConfident working with other members of staff throughout the companyLaboratory experience would be beneficial but not essential as full training will be provided Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Do you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual and as part of a team? We are looking for a Product Test Technician to join a global medical device and healthcare leader based in Witney.This is a 12-month contract with the potential for extension, working 37.5 hours per week, 07:00 - 15:00. The successful candidate will be handling, sampling and testing the finished product. Benefits:Friendly and welcoming teamFree onsite parkingOnsite canteenOutside seating areasWeekly onsite Covid testing available for staffResponsibilities:Perform the set-up, sampling and testing of finished products.Support development/validation trialsSupport product performance monitoring Make sure activities are completed as scheduled on time and in full to meet business and customer's needsAccurate recording and review of data of finished productsPro-actively supporting new/changed procedures, processes, and products within the area, including associated validation/verification activitiesSupporting the design, planning, and delivery of new training materials and the review, evaluation, and delivery of existing training materialsQualifications:Secondary level education including English and MathsRequirements:Good written and oral skills are required to help generate clear and legible documentation and understand technical informationConfident working with other members of staff throughout the companyLaboratory experience would be beneficial but not essential as full training will be provided Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • maidenhead, south east
      • contract
      • £30.00 - £40.00, per hour, Depending on experience
      • randstad cpe
      My client, a leading Pharma Biotech, has a requirement for an experienced Medical Info Associate to join their business at their Maidenhead facility on a 6 Month Contract. As Senior Medical Information Manager, you will:Assisting with the collection and reporting reports of all adverse events/product complaints as defined both by internal SOPs and UK/Irish regulationsCopy approval review/approval for factual accuracy of promotional and informative material through VeevaEnsure all promotional material adheres to both the ABPI Code of Practice and the Medicines Act IPHAReviewing/approving promotional and informational material in line with approved product labellingTo be considered for the role of Senior Medical Information Manager, you will: Educated to degree level in a relevant scientific field Minimum of 3 years industry experience Experience in handling 2nd line MI enquiries and generating standard responses Ability to understand technical, scientific, and medical information Experience of working in Neurology and/or immunology preferred Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      My client, a leading Pharma Biotech, has a requirement for an experienced Medical Info Associate to join their business at their Maidenhead facility on a 6 Month Contract. As Senior Medical Information Manager, you will:Assisting with the collection and reporting reports of all adverse events/product complaints as defined both by internal SOPs and UK/Irish regulationsCopy approval review/approval for factual accuracy of promotional and informative material through VeevaEnsure all promotional material adheres to both the ABPI Code of Practice and the Medicines Act IPHAReviewing/approving promotional and informational material in line with approved product labellingTo be considered for the role of Senior Medical Information Manager, you will: Educated to degree level in a relevant scientific field Minimum of 3 years industry experience Experience in handling 2nd line MI enquiries and generating standard responses Ability to understand technical, scientific, and medical information Experience of working in Neurology and/or immunology preferred Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • witney, south east
      • contract
      • £11.60 per hour
      • randstad business support
      Randstad is recruiting for a Lab Technician on behalf of a global medical device and health care leader, who are dedicated to helping people reach their full health potential. The successful candidate will have great attention to detail, be able to pick up the nature of the role quickly and be able to deliver quality and compliant products in a timely manner.Key Responsibilities:* Perform sampling, inspections, sensor testing, batch record review and approval* Perform inspections associated with laboratory investigations and / or technical / quality system investigations and generate associated reports* To visually inspect products (or with the use of specified instruments) as directed,for defects or imperfections in accordance with the relevant Standard Operating Procedures (SOP's)* Managing the product retain process, placing product lots into applicable storage conditions and coordinating the timely destruction of products at the end of their retention periodKey Requirements:* Excellent attention to detail* Experience in a similar role would be advantageous * Good problem solving abilities* Basic IT skills* Secondary education - Maths and English GCSE Please apply with an up to date CV and we will be in touch shortly. Randstad Business Support is acting as an Employment Business in relation to this vacancy.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      Randstad is recruiting for a Lab Technician on behalf of a global medical device and health care leader, who are dedicated to helping people reach their full health potential. The successful candidate will have great attention to detail, be able to pick up the nature of the role quickly and be able to deliver quality and compliant products in a timely manner.Key Responsibilities:* Perform sampling, inspections, sensor testing, batch record review and approval* Perform inspections associated with laboratory investigations and / or technical / quality system investigations and generate associated reports* To visually inspect products (or with the use of specified instruments) as directed,for defects or imperfections in accordance with the relevant Standard Operating Procedures (SOP's)* Managing the product retain process, placing product lots into applicable storage conditions and coordinating the timely destruction of products at the end of their retention periodKey Requirements:* Excellent attention to detail* Experience in a similar role would be advantageous * Good problem solving abilities* Basic IT skills* Secondary education - Maths and English GCSE Please apply with an up to date CV and we will be in touch shortly. Randstad Business Support is acting as an Employment Business in relation to this vacancy.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • witney, south east
      • temp to perm
      • £10.26 - £10.26, per hour, Additional Benefits
      • randstad inhouse services
      Do you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual? We are looking for Product Return Investigators to join a global medical device and healthcare leader based in Witney.This role involves investigating why a product has been returned using in-house computer systems. You will be investigating the quality of returned products by finding the cause of their faults. Hours and Pay rate: £10.26 per hourMonday to Friday08:00 - 16:00pm (part time available!) Benefits:Full training providedFree on-site parkingOnsite canteen and outside seating areasExcellent long term prospectsFriendly and welcoming teamModern on site facilitiesNewly expanded laboratory settingWeekly onsite Covid testing available for staffResponsibilities:Conduct investigations on customer returned products in accordance with site and divisional proceduresProactively support the implementation of new and / or improved processesCommunicate in a professional manner with colleagues worldwideMeet division goals for timeliness of complaint investigations and identify opportunities for improvement and/or better efficiencies in investigation processes.Conform to all relevant legislation and company Health and Safety policies.Pro-active in recommending improvements in terms of recommending cost savings through complaint process improvements and data quality, in line with Business Excellence initiatives.Keep up to date with the development of new products and through collaboration with peers within the complaints team and across the business, support activities required for complaint readiness prior to product launch. Identifying any trends in product complaints that are found during investigations and highlighting these to managementHandling multiple tasks effectively and efficiently in a team environment with minimal supervisionRequirements:Experience of using computer packages including Word and Excel.5 years of referencing (employment or alternative activity) history will need to be obtained if you are successful in your application. If this is a role you are interested in and you want to work for a renowned healthcare company, don't hesitate, apply today! Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      Do you have excellent written communication skills? Are you computer literate? Are you comfortable working as an individual? We are looking for Product Return Investigators to join a global medical device and healthcare leader based in Witney.This role involves investigating why a product has been returned using in-house computer systems. You will be investigating the quality of returned products by finding the cause of their faults. Hours and Pay rate: £10.26 per hourMonday to Friday08:00 - 16:00pm (part time available!) Benefits:Full training providedFree on-site parkingOnsite canteen and outside seating areasExcellent long term prospectsFriendly and welcoming teamModern on site facilitiesNewly expanded laboratory settingWeekly onsite Covid testing available for staffResponsibilities:Conduct investigations on customer returned products in accordance with site and divisional proceduresProactively support the implementation of new and / or improved processesCommunicate in a professional manner with colleagues worldwideMeet division goals for timeliness of complaint investigations and identify opportunities for improvement and/or better efficiencies in investigation processes.Conform to all relevant legislation and company Health and Safety policies.Pro-active in recommending improvements in terms of recommending cost savings through complaint process improvements and data quality, in line with Business Excellence initiatives.Keep up to date with the development of new products and through collaboration with peers within the complaints team and across the business, support activities required for complaint readiness prior to product launch. Identifying any trends in product complaints that are found during investigations and highlighting these to managementHandling multiple tasks effectively and efficiently in a team environment with minimal supervisionRequirements:Experience of using computer packages including Word and Excel.5 years of referencing (employment or alternative activity) history will need to be obtained if you are successful in your application. If this is a role you are interested in and you want to work for a renowned healthcare company, don't hesitate, apply today! Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • abingdon, south east
      • temporary
      • randstad inhouse services
      Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.The position of Sales Order and Dispatch Specialist is within our Abbott Rapid Diagnostics customer operations department located in Abingdon, Oxfordshire. This role will be working within a team of multi-talented staff providing an excellent service to our customers. The Sales Order Processing team is a fast paced team and the ideal candidate should beable to make quick decisions and have good problem solving skills.This job description will be reviewed periodically and is subject to change by management. Responsibilitie:- Setting up and processing all customer orders and standing orders- Informing customers. Distributors and subsidiary companies of expected deliverydates for orders placed amd prioritizing orders and coordinating shipment- Coordinating the daily despatch of customers' orders amd liasing with the warehouse to arrange succesful delivery- Dealing with ans ressolving complaints and queries from customers, distributors and subsidiary companies regarding order processing. Logging of queries and complaints on our company data base.- Liason with other departments to ensure customer satisfaction- Additional duties include: answering general incoming calls and assisting with Front of House (reception) cover during periods of absence.Qualifications:- Excellent written and oral communication skills- Excellent telephone manner- Good problem solving skills- Good Microsoft Office skills including Word, Excel, Power Point, Outlook- Ability to prioritise workload to meet deadlinesCompetencies:- Able to use own initiative- Willing to help other areas of the team when required- Ability to build strong working relationships- Customer focused
      Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.The position of Sales Order and Dispatch Specialist is within our Abbott Rapid Diagnostics customer operations department located in Abingdon, Oxfordshire. This role will be working within a team of multi-talented staff providing an excellent service to our customers. The Sales Order Processing team is a fast paced team and the ideal candidate should beable to make quick decisions and have good problem solving skills.This job description will be reviewed periodically and is subject to change by management. Responsibilitie:- Setting up and processing all customer orders and standing orders- Informing customers. Distributors and subsidiary companies of expected deliverydates for orders placed amd prioritizing orders and coordinating shipment- Coordinating the daily despatch of customers' orders amd liasing with the warehouse to arrange succesful delivery- Dealing with ans ressolving complaints and queries from customers, distributors and subsidiary companies regarding order processing. Logging of queries and complaints on our company data base.- Liason with other departments to ensure customer satisfaction- Additional duties include: answering general incoming calls and assisting with Front of House (reception) cover during periods of absence.Qualifications:- Excellent written and oral communication skills- Excellent telephone manner- Good problem solving skills- Good Microsoft Office skills including Word, Excel, Power Point, Outlook- Ability to prioritise workload to meet deadlinesCompetencies:- Able to use own initiative- Willing to help other areas of the team when required- Ability to build strong working relationships- Customer focused
      • maidenhead, south east
      • contract
      • £40.00 - £48.00 per hour
      • randstad cpe
      Responsible for all local Pharmacovigilance-related activities for provision of safety report handling relating to Development and maintenance of local PV processes and procedures.As Drug Safety Manager, you will: Reviewing local and national legislation (MHRA or HPRA) to maintain an awareness of local regulations and ensuring local processes are aligned Notifying Global Drug Safety of any programmes/contractual arrangements with external providers with significance for handling AE information Monitoring the MHRA portal for safety reports To be considered for the role of Drug Safety Manager, you will:At least 5 years experience in Drug safety/ Pharmacovigilance in a Pharmaceutical business2 Years in PV Affiliate functionDrafting and Revising safety detailsextensive PV affiliate experience beyond just ICSR managementRSG Database 12 Month Contract, full time. This is an Inside IR35 role, based in Maidenhead. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Responsible for all local Pharmacovigilance-related activities for provision of safety report handling relating to Development and maintenance of local PV processes and procedures.As Drug Safety Manager, you will: Reviewing local and national legislation (MHRA or HPRA) to maintain an awareness of local regulations and ensuring local processes are aligned Notifying Global Drug Safety of any programmes/contractual arrangements with external providers with significance for handling AE information Monitoring the MHRA portal for safety reports To be considered for the role of Drug Safety Manager, you will:At least 5 years experience in Drug safety/ Pharmacovigilance in a Pharmaceutical business2 Years in PV Affiliate functionDrafting and Revising safety detailsextensive PV affiliate experience beyond just ICSR managementRSG Database 12 Month Contract, full time. This is an Inside IR35 role, based in Maidenhead. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Scientist? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! As a scientist you will join our client's Cell Biology Team! The purpose of this role is to conduct scientific work, to support the development and production of animal myoblasts or adipocytes from stem cells to replace muscle or fat grown in animals. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Develop, optimise and characterise stem cell cultures and differentiation protocols to maximise conversion into muscle or fat cellsOptimise protocols for isolation and maintenance of primary stem cells in vitroDesign, plan, and execute complex R&D experiments ensuring that deliverables are successfully met within timelinesDocument research findings clearly in a lab bookCommunicate regularly in group meetings and prepare and deliver presentations to project team and internal stakeholdersAlong with team members, provide routine laboratory maintenance, including participating in equipment upkeep, cleaning rotas and laboratory consumables stock managementShared responsibility for out-of-hours cell culture maintenanceEnsure that laboratory health, safety and quality procedures are followedSelect, follow, and adapt experimental protocols and generate laboratory SOPsSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsMaintain the confidentiality of the project and protocolsKeep abreast of current technologies and relevant scientific literature to help identify opportunity for improvements and reduction of costs Qualifications: Master or PhD in Life Sciences, Biotechnology or related fieldTwo or more years of postdoctoral experience or industry experience in myogenesis or adipogenesis Essential Experience: Extensive experience in muscle or fat biology, with deep knowledge in stem cell biology, cell metabolism and developmentProven experience in cell culture, including maintenance and differentiation of stem cellsSubstantial experience in molecular biology techniques such as PCR, qRT-PCR, Western Blot, Flow cytometry and ImagingAbility to work independently and as part of growing teamSkilled in troubleshooting and conducting multi-factorial experimentsGood numeracy, computer and communication skills Desirable Experience: Experience with cell isolation protocols from biological samplesFamiliarity with co-cultures and 3D culture systemsApplication of Design of Experiments (DoE) to rationalize experiment designExperience of writing SOPs and risk assessmentsRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Scientist? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! As a scientist you will join our client's Cell Biology Team! The purpose of this role is to conduct scientific work, to support the development and production of animal myoblasts or adipocytes from stem cells to replace muscle or fat grown in animals. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Develop, optimise and characterise stem cell cultures and differentiation protocols to maximise conversion into muscle or fat cellsOptimise protocols for isolation and maintenance of primary stem cells in vitroDesign, plan, and execute complex R&D experiments ensuring that deliverables are successfully met within timelinesDocument research findings clearly in a lab bookCommunicate regularly in group meetings and prepare and deliver presentations to project team and internal stakeholdersAlong with team members, provide routine laboratory maintenance, including participating in equipment upkeep, cleaning rotas and laboratory consumables stock managementShared responsibility for out-of-hours cell culture maintenanceEnsure that laboratory health, safety and quality procedures are followedSelect, follow, and adapt experimental protocols and generate laboratory SOPsSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsMaintain the confidentiality of the project and protocolsKeep abreast of current technologies and relevant scientific literature to help identify opportunity for improvements and reduction of costs Qualifications: Master or PhD in Life Sciences, Biotechnology or related fieldTwo or more years of postdoctoral experience or industry experience in myogenesis or adipogenesis Essential Experience: Extensive experience in muscle or fat biology, with deep knowledge in stem cell biology, cell metabolism and developmentProven experience in cell culture, including maintenance and differentiation of stem cellsSubstantial experience in molecular biology techniques such as PCR, qRT-PCR, Western Blot, Flow cytometry and ImagingAbility to work independently and as part of growing teamSkilled in troubleshooting and conducting multi-factorial experimentsGood numeracy, computer and communication skills Desirable Experience: Experience with cell isolation protocols from biological samplesFamiliarity with co-cultures and 3D culture systemsApplication of Design of Experiments (DoE) to rationalize experiment designExperience of writing SOPs and risk assessmentsRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Senior Scientist? Are you looking for a Protein based Team Leader role? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Senior Scientist to work as our client's Protein Sciences Leader. The successful candidate will be utilising their expertise to design and execute protein engineering strategies, source new technologies and implement new assays towards low cost and reproducible manufacture of proteins such as growth factors for cultivated meat. You will work closely with the other R&D teams to optimise protocols and deliver our company-wide milestones.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Advance protein expression, purification, characterisation and analysis capabilitiesDevelop assays for high-throughput screeningSource, evaluate and test growth factors using high-throughput methodologiesEvaluate available technologies for the supplementation and cost reduction of proteins in the mediaDesign, plan, and perform complex experiments to ensure deliverables are successfully met within project timelinesDetermine the most appropriate methodologies to test hypotheses, and identify suitable alternatives if technical problems ariseDocument research findings clearly in an electronic lab bookWrite and further develop experimental protocols and generate laboratory SOPsSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsLead and develop the Protein Sciences team by providing guidance and supportParticipate as a key member of the R&D management team with responsibility for day-to-day decision making within your teamProvide written and verbal progress reports to the Senior Leadership Team and to external collaboratorsKeep up to date with field developments and apply these to improve experimental design and assay performanceQualifications: A PhD in a relevant area of Biochemistry, Molecular Biology or related field≥ 6 years of post-doctoral or industry experience in relevant areaEssential Experience:Extensive experience in producing, purifying proteins and analysing their quality and bioactivityExpertise with analytical techniques and computational approaches to protein engineeringIndustrial experience with assay development, high-throughput screening and protein characterizationStrong background in cellular and molecular biology technical processes such as cell-based activity assays, enzyme-based metabolism assays, immunosorbent assays, protein quantification and protein refoldingProven history of refining protocols and methodologies to reduce cost baseSkilled at the design, set-up and running of complex experimentsProficient in the detailed statistical analysis and presentation of intricate data setsExperience of writing SOPs and risk assessments under quality management systemHighly organised, self-motivated, and capable of working both independently and collaboratively, in a fast-paced team environment with shifting prioritiesSkilled in root cause analysis and problem solvingManagement experience with a proven track record of success delivering R&D projectsStrategic thinker and a history of independent investigations and innovative thinkingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Senior Scientist? Are you looking for a Protein based Team Leader role? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Senior Scientist to work as our client's Protein Sciences Leader. The successful candidate will be utilising their expertise to design and execute protein engineering strategies, source new technologies and implement new assays towards low cost and reproducible manufacture of proteins such as growth factors for cultivated meat. You will work closely with the other R&D teams to optimise protocols and deliver our company-wide milestones.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Advance protein expression, purification, characterisation and analysis capabilitiesDevelop assays for high-throughput screeningSource, evaluate and test growth factors using high-throughput methodologiesEvaluate available technologies for the supplementation and cost reduction of proteins in the mediaDesign, plan, and perform complex experiments to ensure deliverables are successfully met within project timelinesDetermine the most appropriate methodologies to test hypotheses, and identify suitable alternatives if technical problems ariseDocument research findings clearly in an electronic lab bookWrite and further develop experimental protocols and generate laboratory SOPsSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsLead and develop the Protein Sciences team by providing guidance and supportParticipate as a key member of the R&D management team with responsibility for day-to-day decision making within your teamProvide written and verbal progress reports to the Senior Leadership Team and to external collaboratorsKeep up to date with field developments and apply these to improve experimental design and assay performanceQualifications: A PhD in a relevant area of Biochemistry, Molecular Biology or related field≥ 6 years of post-doctoral or industry experience in relevant areaEssential Experience:Extensive experience in producing, purifying proteins and analysing their quality and bioactivityExpertise with analytical techniques and computational approaches to protein engineeringIndustrial experience with assay development, high-throughput screening and protein characterizationStrong background in cellular and molecular biology technical processes such as cell-based activity assays, enzyme-based metabolism assays, immunosorbent assays, protein quantification and protein refoldingProven history of refining protocols and methodologies to reduce cost baseSkilled at the design, set-up and running of complex experimentsProficient in the detailed statistical analysis and presentation of intricate data setsExperience of writing SOPs and risk assessments under quality management systemHighly organised, self-motivated, and capable of working both independently and collaboratively, in a fast-paced team environment with shifting prioritiesSkilled in root cause analysis and problem solvingManagement experience with a proven track record of success delivering R&D projectsStrategic thinker and a history of independent investigations and innovative thinkingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Senior Scientist? Are you looking for a Team Leader role? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Senior Scientist to work as our clients Culture Medium Team Leader. Your primary focus is to develop culture medium formulations using high-throughput technology towards animal component free, low cost, large-scale and reproducible manufacture of cultivated meat. You will work closely with the other R&D teams to optimise protocols and deliver our company-wide milestones.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Design, plan, and perform R&D Culture Medium activities, ensuring that deliverables are successfully met within project timelinesLead and develop the Culture Medium team to deliver on R&D milestonesProvide guidance and coaching to support the growth of the Culture medium teamDetermine the most appropriate methodologies to test hypotheses, and identify suitable alternatives if technical problems ariseGather, analyse, and present scientific data from a variety of sourcesDocument research findings clearly in an electronic lab bookSelect, follow, and further develop experimental protocols and generate laboratory SOPsProvide general laboratory management and administrationSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsParticipate as a key member of the R&D management team with responsibility for day-to-day decision making within your teamProvide written and verbal progress reports to the Senior Leadership Team and to external collaboratorsContribute to discussions and share research findings with colleagues in partner institutions, and research groups (as required)Keep up to date with field developments and apply these to improve experimental design and assay performanceQualifications: A PhD in a relevant area of Biological Sciences or related field≥ 6 years of post-doctoral or industry experience in relevant areaEssential experience required: In-depth experience in cell culture: isolation, maintenance and differentiation of stem or primary cell typesExpertise in cellular and molecular biology assays such as enzyme-based metabolism assays, protein quantification, ICH & PCRProven experience in the development of cell-based processes, including in-depth expertise in cultured cell biochemistry, metabolism and culture medium developmentSkilled at the design, set up and running of complex experimentsProficient in the detailed analysis and presentation of complex data setsMathematically literateFamiliarity with the development and implementation of automation to support high-throughput media developmentExperience of writing SOPs and risk assessments under quality management systemHighly organised, self-motivated, and capable of working both independently and collaboratively, in a fast-paced team environment with shifting prioritiesRoot cause analysis and problem solvingManagement experience with a proven track record of success delivering R&D projectsA proven history of independent investigations and innovative thinkingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Senior Scientist? Are you looking for a Team Leader role? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Senior Scientist to work as our clients Culture Medium Team Leader. Your primary focus is to develop culture medium formulations using high-throughput technology towards animal component free, low cost, large-scale and reproducible manufacture of cultivated meat. You will work closely with the other R&D teams to optimise protocols and deliver our company-wide milestones.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Design, plan, and perform R&D Culture Medium activities, ensuring that deliverables are successfully met within project timelinesLead and develop the Culture Medium team to deliver on R&D milestonesProvide guidance and coaching to support the growth of the Culture medium teamDetermine the most appropriate methodologies to test hypotheses, and identify suitable alternatives if technical problems ariseGather, analyse, and present scientific data from a variety of sourcesDocument research findings clearly in an electronic lab bookSelect, follow, and further develop experimental protocols and generate laboratory SOPsProvide general laboratory management and administrationSupport the preparation of laboratory risk assessments and maintenance of health and safety protocolsParticipate as a key member of the R&D management team with responsibility for day-to-day decision making within your teamProvide written and verbal progress reports to the Senior Leadership Team and to external collaboratorsContribute to discussions and share research findings with colleagues in partner institutions, and research groups (as required)Keep up to date with field developments and apply these to improve experimental design and assay performanceQualifications: A PhD in a relevant area of Biological Sciences or related field≥ 6 years of post-doctoral or industry experience in relevant areaEssential experience required: In-depth experience in cell culture: isolation, maintenance and differentiation of stem or primary cell typesExpertise in cellular and molecular biology assays such as enzyme-based metabolism assays, protein quantification, ICH & PCRProven experience in the development of cell-based processes, including in-depth expertise in cultured cell biochemistry, metabolism and culture medium developmentSkilled at the design, set up and running of complex experimentsProficient in the detailed analysis and presentation of complex data setsMathematically literateFamiliarity with the development and implementation of automation to support high-throughput media developmentExperience of writing SOPs and risk assessments under quality management systemHighly organised, self-motivated, and capable of working both independently and collaboratively, in a fast-paced team environment with shifting prioritiesRoot cause analysis and problem solvingManagement experience with a proven track record of success delivering R&D projectsA proven history of independent investigations and innovative thinkingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Research and Development Project Manager? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Project Manager to work in our clients R&D team, you will proactively contribute to the consistent on-time delivery of R&D projects from Cell Biology to Bioprocessing. Your responsibilities include monitoring and communicating the status of R&D projects to the leadership Team and ensure these are completed within the expected timeframe.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Plan project timelines, project tasks and follow projects their entire lifecycleExecute strategy for ensuring success of new and on-going projects within agreed timelines, budget, scope and internal customer expectationsEnsure all necessary resources are identified and availableLead regular project meetings with internal and external collaboratorsCommunicate timely project updates and progress to the leadership teamUse a mix of creative and established tools to manage and communicate effectivelyIdentify, manage and mitigate project risks and obstaclesManage changes in project scope, timelines, and prioritiesGenerate and circulate of project status, cycle time and on-time delivery performance reportsUndertakes improvement projects and ad hoc tasksHelps establish standard operating procedures that drive repeatability and consistencyLead CAPA investigations to identify root cause of errors/failure and formulate recommendations to learn, adapt and prevent recurrenceQualifications: Degree in Life Sciences, Biochemistry, Biotechnology or related fieldEssential ExperienceIn depth understanding of project management principles and project lifecycle methodologiesAgile, Prince 2, PMP - or equivalent knowledge in Project Management methodologiesExtensive experience in working in a scientific environment planning, scheduling and completing successful projects with cross-functional teamsExcellent track record for managing internal and external projects within budgetAbility to manage complex projects under pressure and to tight deadlinesAbility prioritise tasks and time efficientlyExcellent risk management and mitigation to ensure timely project deliveryHighly organized, self-motivated, and capable of working both independently and collaboratively; in a fast-paced team environment with shifting prioritiesStrong excel and data interpretation skills and suitable attention to detailExcellent verbal and written communication skills, ability to present complex ideas to a variety of audiencesDesirable ExperienceExperienced in applying process improvement methodologies such as Lean, 6 Sigma, Kanban, PDSA, Root causeExperience in working with stem cells and tissue engineeringRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Research and Development Project Manager? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Project Manager to work in our clients R&D team, you will proactively contribute to the consistent on-time delivery of R&D projects from Cell Biology to Bioprocessing. Your responsibilities include monitoring and communicating the status of R&D projects to the leadership Team and ensure these are completed within the expected timeframe.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Plan project timelines, project tasks and follow projects their entire lifecycleExecute strategy for ensuring success of new and on-going projects within agreed timelines, budget, scope and internal customer expectationsEnsure all necessary resources are identified and availableLead regular project meetings with internal and external collaboratorsCommunicate timely project updates and progress to the leadership teamUse a mix of creative and established tools to manage and communicate effectivelyIdentify, manage and mitigate project risks and obstaclesManage changes in project scope, timelines, and prioritiesGenerate and circulate of project status, cycle time and on-time delivery performance reportsUndertakes improvement projects and ad hoc tasksHelps establish standard operating procedures that drive repeatability and consistencyLead CAPA investigations to identify root cause of errors/failure and formulate recommendations to learn, adapt and prevent recurrenceQualifications: Degree in Life Sciences, Biochemistry, Biotechnology or related fieldEssential ExperienceIn depth understanding of project management principles and project lifecycle methodologiesAgile, Prince 2, PMP - or equivalent knowledge in Project Management methodologiesExtensive experience in working in a scientific environment planning, scheduling and completing successful projects with cross-functional teamsExcellent track record for managing internal and external projects within budgetAbility to manage complex projects under pressure and to tight deadlinesAbility prioritise tasks and time efficientlyExcellent risk management and mitigation to ensure timely project deliveryHighly organized, self-motivated, and capable of working both independently and collaboratively; in a fast-paced team environment with shifting prioritiesStrong excel and data interpretation skills and suitable attention to detailExcellent verbal and written communication skills, ability to present complex ideas to a variety of audiencesDesirable ExperienceExperienced in applying process improvement methodologies such as Lean, 6 Sigma, Kanban, PDSA, Root causeExperience in working with stem cells and tissue engineeringRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Product Development Chef? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Product Development Chef, the successful candidate will be the culinary leader for our client, maintaining close links with R&D, product development and marketing. You will provide knowledge on trends and competitor activity to the rest of the business and be a stellar technical project manager. You will be required to be our public face and understand our products and be able to confidently explain their quality and nutrition both internally and externally. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Be the culinary leader for our client - maintain close links with R&D, product development and marketingProvide knowledge on trends and competitor activity to the rest of the business Be a public face of our client - understand our products and be able to confidently explain their quality and nutrition both internally and externally Use deep understanding of consumers to develop perceived high-quality products within any cost, sustainability or nutritional constraintsBe able to co-create new ideas with product development colleagues Provide relevant digital content such as recipe suggestions and cooking hacks Ensure the kitchen is maintained in good condition, is well stocked and all health & safety aspects are adhered to Carry out relevant sensory studies to ensure our products perform well Understand key ingredient functionality and the impact of manufacturing processes for scaling Understand competitor products and options to achieve competitive advantage (including claims) Good nutritional understanding and ability to provide evidence to back up any claims Accurate data management, including specifications and recipe systems Ensure all products in range are safe, legal and meet all brand requirements Technical project management to ensure milestones are met and projects are kept within budgetEssential experience required: High level culinary qualificationHigh-end restaurant experienceMinimum 3 years product development experience within food FMCGEstablished network within food industry - ingredients suppliers, manufacturers and retail / foodservice partnersGood nutritional understanding and able to translate consumer insights into winning productsSensory knowledgeProject management skillsIngredient functionality expertiseSpecifications and recipe systems expertiseA resourceful self-starter Desirable:Experience working with meat alternatives category Membership of professional culinary body Media experience Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Product Development Chef? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This role is for a Product Development Chef, the successful candidate will be the culinary leader for our client, maintaining close links with R&D, product development and marketing. You will provide knowledge on trends and competitor activity to the rest of the business and be a stellar technical project manager. You will be required to be our public face and understand our products and be able to confidently explain their quality and nutrition both internally and externally. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Be the culinary leader for our client - maintain close links with R&D, product development and marketingProvide knowledge on trends and competitor activity to the rest of the business Be a public face of our client - understand our products and be able to confidently explain their quality and nutrition both internally and externally Use deep understanding of consumers to develop perceived high-quality products within any cost, sustainability or nutritional constraintsBe able to co-create new ideas with product development colleagues Provide relevant digital content such as recipe suggestions and cooking hacks Ensure the kitchen is maintained in good condition, is well stocked and all health & safety aspects are adhered to Carry out relevant sensory studies to ensure our products perform well Understand key ingredient functionality and the impact of manufacturing processes for scaling Understand competitor products and options to achieve competitive advantage (including claims) Good nutritional understanding and ability to provide evidence to back up any claims Accurate data management, including specifications and recipe systems Ensure all products in range are safe, legal and meet all brand requirements Technical project management to ensure milestones are met and projects are kept within budgetEssential experience required: High level culinary qualificationHigh-end restaurant experienceMinimum 3 years product development experience within food FMCGEstablished network within food industry - ingredients suppliers, manufacturers and retail / foodservice partnersGood nutritional understanding and able to translate consumer insights into winning productsSensory knowledgeProject management skillsIngredient functionality expertiseSpecifications and recipe systems expertiseA resourceful self-starter Desirable:Experience working with meat alternatives category Membership of professional culinary body Media experience Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Bioprocess Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This position will focus on the design, building, testing, and scale-up of the upstream unit operations centered around animal cell culture and recovery operations. The role will require a strong background in bioreactor design, theory and operation as well as bioprocess equipment and facility design in general. Initially, this Engineer will assist the design and fabrication of prototypes for testing but with the ultimate goal of scaling up this equipment for our future cost-effective commercial-scale manufacturing facilities. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Work with bioprocess development colleagues to identify and define process and system requirements and translate into detailed equipment specificationsDesign and manage fabrication of the upstream process equipment towards robust and highly-dependable aseptic processing by using the appropriate design standards, level of control and automationDesign the upstream portion of manufacturing to ensure reliable and safe operation while also producing a high-quality product free of contaminants while also achieving overall operational efficiencyGenerate process and cost models to identify key drivers of cost and efficiencyManaging relationships while working with strategic partners, engineering firms, equipment vendors and technology partners towards the design, construct and commission Ivy Farm's manufacturing facilitiesSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsSome travel may be required to collaborator and manufacturing sitesQualifications: Bachelor's degree or higher in Engineering, Food Science or related fieldMaster's degree preferred3+ years of related experience in bioprocess equipment design, modeling, facility design, construction, start up and/or operationExperience: Demonstrated strong technical background and ability to lead technically driven projectsAbility to apply biochemical engineering principles and computer-aided methods to equipment design, fabrication, and operationUnderstanding of aseptic techniques and control of microbial contaminationKnowledge of process and facility design and economicsProject engineering and management, including direct management of architectural and engineering design firms, equipment vendors and construction contractorsAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsMechanical aptitude and comfortable with working directly on process equipment and control systemsStrong scientific and technical writing and presentationsDetail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shooting Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Bioprocess Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!This position will focus on the design, building, testing, and scale-up of the upstream unit operations centered around animal cell culture and recovery operations. The role will require a strong background in bioreactor design, theory and operation as well as bioprocess equipment and facility design in general. Initially, this Engineer will assist the design and fabrication of prototypes for testing but with the ultimate goal of scaling up this equipment for our future cost-effective commercial-scale manufacturing facilities. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Work with bioprocess development colleagues to identify and define process and system requirements and translate into detailed equipment specificationsDesign and manage fabrication of the upstream process equipment towards robust and highly-dependable aseptic processing by using the appropriate design standards, level of control and automationDesign the upstream portion of manufacturing to ensure reliable and safe operation while also producing a high-quality product free of contaminants while also achieving overall operational efficiencyGenerate process and cost models to identify key drivers of cost and efficiencyManaging relationships while working with strategic partners, engineering firms, equipment vendors and technology partners towards the design, construct and commission Ivy Farm's manufacturing facilitiesSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsSome travel may be required to collaborator and manufacturing sitesQualifications: Bachelor's degree or higher in Engineering, Food Science or related fieldMaster's degree preferred3+ years of related experience in bioprocess equipment design, modeling, facility design, construction, start up and/or operationExperience: Demonstrated strong technical background and ability to lead technically driven projectsAbility to apply biochemical engineering principles and computer-aided methods to equipment design, fabrication, and operationUnderstanding of aseptic techniques and control of microbial contaminationKnowledge of process and facility design and economicsProject engineering and management, including direct management of architectural and engineering design firms, equipment vendors and construction contractorsAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsMechanical aptitude and comfortable with working directly on process equipment and control systemsStrong scientific and technical writing and presentationsDetail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shooting Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Mechanical Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!As the Extrusion and Food Process Engineer, you will be the first member of the Bioprocess Engineering group that will be responsible for the design and implementation of our clients first-of-its-kind manufacturing processes and facilities. This position will design, build, test, and scale-up mechanical process equipment for cold extrusion and other specialty process applications. The role will require a strong background in machine design with the ultimate goal of deploying this equipment in our future commercial-scale manufacturing facilities and bringing strategic differentiation to our production platform.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Identify and define process and system requirements by understanding and challenging product formulation and processing assumptions with the aim of implementing robust unit operations and increasing overall operational efficiency and effectivenessPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsManaging relationships with strategic partners, engineering firms, equipment vendors and technology partnersSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsSome travel may be required to collaborator and manufacturing sitesAdditional ad hoc duties as required by the companyExperience: Ability to apply mechanical engineering principles and computer-aided methods to machine design and fabricationMechanical aptitude and comfortable with working directly on mechanical equipmentEfficient Design of Experiments and statistical analysis of experimental and characterization/validation dataUnderstanding of aseptic techniques and control of microbial contaminationAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsProject engineering and managementStrong scientific and technical writing and presentations.Detail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shootingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Mechanical Design Engineer? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!As the Extrusion and Food Process Engineer, you will be the first member of the Bioprocess Engineering group that will be responsible for the design and implementation of our clients first-of-its-kind manufacturing processes and facilities. This position will design, build, test, and scale-up mechanical process equipment for cold extrusion and other specialty process applications. The role will require a strong background in machine design with the ultimate goal of deploying this equipment in our future commercial-scale manufacturing facilities and bringing strategic differentiation to our production platform.This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Identify and define process and system requirements by understanding and challenging product formulation and processing assumptions with the aim of implementing robust unit operations and increasing overall operational efficiency and effectivenessPartner with internal and external teams to solve technical challenges and identify opportunities for process improvement and cost savingsManaging relationships with strategic partners, engineering firms, equipment vendors and technology partnersSpecify project scope, timelines, resourcing and budget needsDevelop project capital requirements and objectives through creation of proposals and plans with breakdown structures (WBS)Track and complete projects by managing schedules, costs and specificationsSome travel may be required to collaborator and manufacturing sitesAdditional ad hoc duties as required by the companyExperience: Ability to apply mechanical engineering principles and computer-aided methods to machine design and fabricationMechanical aptitude and comfortable with working directly on mechanical equipmentEfficient Design of Experiments and statistical analysis of experimental and characterization/validation dataUnderstanding of aseptic techniques and control of microbial contaminationAbility to partner cross-functionally on proprietary process technologies, while also developing and leveraging successful external contacts and relationshipsProject engineering and managementStrong scientific and technical writing and presentations.Detail oriented with excellent verbal and written communication skillsInnovative and creative thinking and willing to challenge established methods and beliefsSelf-starter with a strong bias for action and ability for problem-solving and trouble-shootingRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • oxford, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Research Associate? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!The Research Associate will be working to to support the development of exciting new technologies to tackle a range of challenges associated with making our client's vision a reality. This is a lab-based role where you will be supporting the delivery of our research goals, the purpose of this role is to conduct scientific work to support the development of innovative technologies & processes. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Generate hypothesis and execute experiments related to R&D activities Analyse empirical data to identify significant results Feedback and present results to team Prepare reagents and perform analytical testing Generate SOPs, COSHH and other risk assessment documents  Participate in group R&D meetings  Maintain and organise laboratory consumables, reagents and equipment inventory  Ensure accurate recording of all experiments using electronic laboratory notebook  Laboratory maintenance (rota system)  Maintain the confidentiality of the project and protocols Qualifications: Degree in Life sciences, Genetics, Biotechnology, Biochemistry, Bioprocessing, Bioengineering, Material Science, Polymer Chemistry or related fieldExperience: Good understanding in the principles of your discipline Laboratory experience - at least one individual or shared project (including design and implementation of experiments) Good numeracy and problem-solving abilities Ability to communicate with a multi-disciplinary team Computer literate and ability to learn new software platforms Experience of experimental record-keeping Critical assessment of research articles  Data processing and statistical analysis And experience in one or more areas: Aseptic mammalian cell culture experience for adherent and/or suspension cell lines.  Molecular biology skillset in either DNA, protein or lipid characterisation Analysis of nutrient or metabolite content in culture media Experience in tissue engineering and/or working with biomaterials Set-up, running and harvesting of bioreactor Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Research Associate? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you!The Research Associate will be working to to support the development of exciting new technologies to tackle a range of challenges associated with making our client's vision a reality. This is a lab-based role where you will be supporting the delivery of our research goals, the purpose of this role is to conduct scientific work to support the development of innovative technologies & processes. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities:Generate hypothesis and execute experiments related to R&D activities Analyse empirical data to identify significant results Feedback and present results to team Prepare reagents and perform analytical testing Generate SOPs, COSHH and other risk assessment documents  Participate in group R&D meetings  Maintain and organise laboratory consumables, reagents and equipment inventory  Ensure accurate recording of all experiments using electronic laboratory notebook  Laboratory maintenance (rota system)  Maintain the confidentiality of the project and protocols Qualifications: Degree in Life sciences, Genetics, Biotechnology, Biochemistry, Bioprocessing, Bioengineering, Material Science, Polymer Chemistry or related fieldExperience: Good understanding in the principles of your discipline Laboratory experience - at least one individual or shared project (including design and implementation of experiments) Good numeracy and problem-solving abilities Ability to communicate with a multi-disciplinary team Computer literate and ability to learn new software platforms Experience of experimental record-keeping Critical assessment of research articles  Data processing and statistical analysis And experience in one or more areas: Aseptic mammalian cell culture experience for adherent and/or suspension cell lines.  Molecular biology skillset in either DNA, protein or lipid characterisation Analysis of nutrient or metabolite content in culture media Experience in tissue engineering and/or working with biomaterials Set-up, running and harvesting of bioreactor Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • kidlington, south east
      • permanent
      • randstad cpe
      Are you looking for a new role as a Facilities Manager? Do you have experience in looking after highly regulated sites? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! This is a new role, supporting the move to a new facility whilst ensuring that all facilities are managed and delivered in a quality and cost-conscious way. Working within an agreed budget and managing all outsourced facility providers to maintain the building fabric, plant and grounds of site. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Own and manage contracts and relationships with external facility suppliers, including but not limited to utilities, cleaning, refuse collection, lab waste collection, telephony, broadband and laundry Take a lead for site Health & Safety, fire alarms, security systems including managing the maintenance and regular drills and testing. Staying up to date with all relative legislation and procedures Working closely with R&D team and Laboratory Associate to ensure Laboratory maintenance, H&S, and consumables stock are compliant and well managed Management of on-site equipment, including maintaining database of all equipment, ensuring regular compliance testing (PAT) and keeping all associated records and documentation Responsibility for managing building repairs and maintenance (including planned preventative) through a network of contractors Oversee business support functions and activities including reception, office administration & ordering and stock management Manage relationship with Oxford Business Park management and security teams Be on call to deal with emergency situations out of hours Keep and be able to interpret technical drawings and schematics for the site Other ad hoc duties as required Experience: Minimum 10 years' proven experience in a similar role(s) Proven ability to manage complex building related issues Demonstrable knowledge of laboratory safety and health and safety at work regulationsFire warden, first aider in previous roles Very good written and verbal communication skills Be resilient and able to work well under pressure, prioritise a heavy workload and work both reactively and proactively Organised and accurate with a strong focus on attention to detailExcellent people skills with the ability to interact with a wide range of customer and Management needs Previous experience in managing contractor teams and staff Keeps up to date with professional knowledge, expertise and best practice A good team player with a hands on approachRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Are you looking for a new role as a Facilities Manager? Do you have experience in looking after highly regulated sites? Do you want to work for a business that is growing at a rapid pace with lots of opportunity for the future? If so, this could be the role for you! This is a new role, supporting the move to a new facility whilst ensuring that all facilities are managed and delivered in a quality and cost-conscious way. Working within an agreed budget and managing all outsourced facility providers to maintain the building fabric, plant and grounds of site. This role is offered on a full time permanent basis, with a business that also offers lots of other benefits that will make you feel truly at home whilst at work. Responsibilities: Own and manage contracts and relationships with external facility suppliers, including but not limited to utilities, cleaning, refuse collection, lab waste collection, telephony, broadband and laundry Take a lead for site Health & Safety, fire alarms, security systems including managing the maintenance and regular drills and testing. Staying up to date with all relative legislation and procedures Working closely with R&D team and Laboratory Associate to ensure Laboratory maintenance, H&S, and consumables stock are compliant and well managed Management of on-site equipment, including maintaining database of all equipment, ensuring regular compliance testing (PAT) and keeping all associated records and documentation Responsibility for managing building repairs and maintenance (including planned preventative) through a network of contractors Oversee business support functions and activities including reception, office administration & ordering and stock management Manage relationship with Oxford Business Park management and security teams Be on call to deal with emergency situations out of hours Keep and be able to interpret technical drawings and schematics for the site Other ad hoc duties as required Experience: Minimum 10 years' proven experience in a similar role(s) Proven ability to manage complex building related issues Demonstrable knowledge of laboratory safety and health and safety at work regulationsFire warden, first aider in previous roles Very good written and verbal communication skills Be resilient and able to work well under pressure, prioritise a heavy workload and work both reactively and proactively Organised and accurate with a strong focus on attention to detailExcellent people skills with the ability to interact with a wide range of customer and Management needs Previous experience in managing contractor teams and staff Keeps up to date with professional knowledge, expertise and best practice A good team player with a hands on approachRandstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • maidenhead, south east
      • temporary
      • randstad business support
      JOB TITLE:Regulatory Affairs Specialist DURATION: 12 Month contract LOCATION: Maidenhead (Can consider WFH flexibility) PAY: £40K-£45K (Dependent on experience)The ClientOn behalf of our client , who is a Global Healthcare provider , Randstad is recruiting for an individual who has a strong background in Regulatory Affairs, to sit in the role as 'Regulatory Affairs Specialist'. There are various divisions within our client- nutrition, diabetes, diagnostics- this sits within nutrition departmentThe Role Support regulatory strategy for registration and reimbursement of new products, taking into account business strategy and regulatory requirements.Ensure maintenance of in-line products.Monitor and implement new regulations to support business maintenance and growth. Support assessment of impact of upcoming regulations in the clients products to use for external engagement through Trade Associations.ResponsibilitiesProduct registration, and reimbursement, launch and maintenance. Support product registration and approval (assessment of formulas, advice on product category, handling tactics and submission timing, verification of label claims, setting mitigation plans, etc.) Negotiate with regulatory authorities during the review process to ensure registration and reimbursement approval. Effectively participate in project teams and ensure timely completion of tasks and clear communication of regulatory risks and opportunities. Ensure implementation of new regulations/guidance within legal deadlines. Approval of labels, datasheets, advertising and promo materials ensuring alignment with local regulations, Codes of Conduct, SOPs,etc. Provides technical and regulatory support to internal stakeholders. Assess and communicate impact of relevant regional regulations/standards in the local market. Administer /meet regulatory requirements to achieve excellent compliance status with no enforcement actions. Must assure that all deadlines are met. The CandidateIndividuals are able to work independently. Completed work is reviewed from a relatively long- term perspective for desired results. Individual is recognized as an industry expert and resource in regulatory affairs. Provides technical leadership to relevant departments. Desired to have a Bachelor's degree (or equivalent) in science (biology, chemistry, microbiology, medical technology, pharmacy, pharmacology, etc.) Regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related areas. Excellent written English and communication skills. Highly developed project management skills.Excellent problem solving skills. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      JOB TITLE:Regulatory Affairs Specialist DURATION: 12 Month contract LOCATION: Maidenhead (Can consider WFH flexibility) PAY: £40K-£45K (Dependent on experience)The ClientOn behalf of our client , who is a Global Healthcare provider , Randstad is recruiting for an individual who has a strong background in Regulatory Affairs, to sit in the role as 'Regulatory Affairs Specialist'. There are various divisions within our client- nutrition, diabetes, diagnostics- this sits within nutrition departmentThe Role Support regulatory strategy for registration and reimbursement of new products, taking into account business strategy and regulatory requirements.Ensure maintenance of in-line products.Monitor and implement new regulations to support business maintenance and growth. Support assessment of impact of upcoming regulations in the clients products to use for external engagement through Trade Associations.ResponsibilitiesProduct registration, and reimbursement, launch and maintenance. Support product registration and approval (assessment of formulas, advice on product category, handling tactics and submission timing, verification of label claims, setting mitigation plans, etc.) Negotiate with regulatory authorities during the review process to ensure registration and reimbursement approval. Effectively participate in project teams and ensure timely completion of tasks and clear communication of regulatory risks and opportunities. Ensure implementation of new regulations/guidance within legal deadlines. Approval of labels, datasheets, advertising and promo materials ensuring alignment with local regulations, Codes of Conduct, SOPs,etc. Provides technical and regulatory support to internal stakeholders. Assess and communicate impact of relevant regional regulations/standards in the local market. Administer /meet regulatory requirements to achieve excellent compliance status with no enforcement actions. Must assure that all deadlines are met. The CandidateIndividuals are able to work independently. Completed work is reviewed from a relatively long- term perspective for desired results. Individual is recognized as an industry expert and resource in regulatory affairs. Provides technical leadership to relevant departments. Desired to have a Bachelor's degree (or equivalent) in science (biology, chemistry, microbiology, medical technology, pharmacy, pharmacology, etc.) Regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related areas. Excellent written English and communication skills. Highly developed project management skills.Excellent problem solving skills. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • maidenhead, south east
      • contract
      • £50.00 - £62.00, per hour, Depending on experience
      • randstad cpe
      My client, a leading pharma Biotech has an exciting opportunity for an experienced Regulatory Affairs manager to join their Asia focused Regulatory development team.As Senior RA Manager, you will:Lead regulatory strategy development for R&D portfolios and marketed products LCM for assigned projectsLead CTA & NDA/BLA filings, and CDE consultation preparation activities by working with Agents/ Third Parties/ CRO, and provide supervision to CRO project responsible, to ensure timely Regulatory filings and response to HA queriesRepresent RA and provide regulatory strategy input to support successful LCM of marketed products including line extensions and variations, and provide Regulatory expertise to local product and cross-functional teamsTo be considered for the role of Senior RA Manager, you will:Educated to degree level in a related scientific fieldMore than 10 years in drug R&D field, minimum of 5-8 years regulatory affair experience in a multinational pharmaceutical companyExperience of China / EMEA regulatory Very strong strategic background, leading activities with agencies and third parties This is a 12 Month Inside IR35 PAYE Contract. Head office in Maidenhead, flexible remote working opportunity. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      My client, a leading pharma Biotech has an exciting opportunity for an experienced Regulatory Affairs manager to join their Asia focused Regulatory development team.As Senior RA Manager, you will:Lead regulatory strategy development for R&D portfolios and marketed products LCM for assigned projectsLead CTA & NDA/BLA filings, and CDE consultation preparation activities by working with Agents/ Third Parties/ CRO, and provide supervision to CRO project responsible, to ensure timely Regulatory filings and response to HA queriesRepresent RA and provide regulatory strategy input to support successful LCM of marketed products including line extensions and variations, and provide Regulatory expertise to local product and cross-functional teamsTo be considered for the role of Senior RA Manager, you will:Educated to degree level in a related scientific fieldMore than 10 years in drug R&D field, minimum of 5-8 years regulatory affair experience in a multinational pharmaceutical companyExperience of China / EMEA regulatory Very strong strategic background, leading activities with agencies and third parties This is a 12 Month Inside IR35 PAYE Contract. Head office in Maidenhead, flexible remote working opportunity. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • petersfield, south east
      • permanent
      • £32,000 - £38,000, per year, Depending on experience
      • randstad cpe
      My client, a leading independent Pharmaceutical business, has a requirement for an experienced Regulatory Affairs officer to join their growing team on a permanent basis.As Senior Regulatory Affairs Officer, you will:Compilation, preparation and review & submission of dossiers, MA Authorisations, variation and compilations of Clinical Trial Applications CTALiaise with regulatory agencies and authorities to facilitate approval of CTAsKeeping up to date on legislation and guidance for EU Directives, especially GMP, GDP, controlled drugsMaintain awareness of the company's quality assurance which comply with GMP, GDP, GCP and GVP - provide support for quality reviews, CAPAs and SOPs as neededTo be considered for the role of Senior Regulatory Affairs Officer, you will:Minimum 2 years related experience within regulatory affairsEducated to degree level in related scientific field MA Variation authoring and EU/ Uk Lifecycle experience Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      My client, a leading independent Pharmaceutical business, has a requirement for an experienced Regulatory Affairs officer to join their growing team on a permanent basis.As Senior Regulatory Affairs Officer, you will:Compilation, preparation and review & submission of dossiers, MA Authorisations, variation and compilations of Clinical Trial Applications CTALiaise with regulatory agencies and authorities to facilitate approval of CTAsKeeping up to date on legislation and guidance for EU Directives, especially GMP, GDP, controlled drugsMaintain awareness of the company's quality assurance which comply with GMP, GDP, GCP and GVP - provide support for quality reviews, CAPAs and SOPs as neededTo be considered for the role of Senior Regulatory Affairs Officer, you will:Minimum 2 years related experience within regulatory affairsEducated to degree level in related scientific field MA Variation authoring and EU/ Uk Lifecycle experience Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • queenborough, south east
      • permanent
      • £45,000 - £55,000 per year
      • randstad cpe
      Quality Specialist required by my client, a Pharmaceutical Manufacturing business based in Kent. You will manage QMS System Owner for all Deviations, CAPAs, Audits, PQRs, ComplaintsCustomer first line quality contact. Attend customer meetings and work with the business to implement customer requirementsTo work with QPs and Development to assist in driving continuous quality improvements.To be considered for the role of Quality Specialist, you will:Demonstrate a good understanding of GMP for IMP and developmentEducated to Science degree or equivalentERP software experience preferable.This is a permanent role, based in Queenborough. Relocation assistance available Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      Quality Specialist required by my client, a Pharmaceutical Manufacturing business based in Kent. You will manage QMS System Owner for all Deviations, CAPAs, Audits, PQRs, ComplaintsCustomer first line quality contact. Attend customer meetings and work with the business to implement customer requirementsTo work with QPs and Development to assist in driving continuous quality improvements.To be considered for the role of Quality Specialist, you will:Demonstrate a good understanding of GMP for IMP and developmentEducated to Science degree or equivalentERP software experience preferable.This is a permanent role, based in Queenborough. Relocation assistance available Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • queenborough, south east
      • permanent
      • £45,000 - £55,000, per year, Relocation Package
      • randstad cpe
      My client, a leading pharmaceutical manufacturer/ CDMO, has a great opportunity for an experienced Regulatory Affairs Specialist to join their team in Kent in Queenborough. As Regulatory Affairs Specialist, you will: License maintenance and variations processes in place and continuously improvedSite registrations processes in place and continuously improvedProduct registrations in compliance with details registered by Marketing Authorisation Holder Management of Regulatory activities to meet legal and company standards consistent with the manufacture of formulated products. Ensure that expert know how exists within the Regulatory Team to ensure that the Regulatory Strategy is clear To be considered for the role of Regulatory Affairs specialist, you will:Educated to degree level in Science Subject or equivalent At least 10 year's experience in a pharmaceutical Regulatory, QMS, QC, QA or Clinical environment Excellent working knowledge of the Finished Dose and the regulatory requirements of the Pharmaceutical industry, including requirements relating to the MHRA, FDA & EMA regulations. A thorough understanding of CGMP requirements is also essential. Significant pharmaceutical compliance and a comprehensive understanding of Regulatory requirements are essentialThis is a permanent position based in Queenborough, Kent. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      My client, a leading pharmaceutical manufacturer/ CDMO, has a great opportunity for an experienced Regulatory Affairs Specialist to join their team in Kent in Queenborough. As Regulatory Affairs Specialist, you will: License maintenance and variations processes in place and continuously improvedSite registrations processes in place and continuously improvedProduct registrations in compliance with details registered by Marketing Authorisation Holder Management of Regulatory activities to meet legal and company standards consistent with the manufacture of formulated products. Ensure that expert know how exists within the Regulatory Team to ensure that the Regulatory Strategy is clear To be considered for the role of Regulatory Affairs specialist, you will:Educated to degree level in Science Subject or equivalent At least 10 year's experience in a pharmaceutical Regulatory, QMS, QC, QA or Clinical environment Excellent working knowledge of the Finished Dose and the regulatory requirements of the Pharmaceutical industry, including requirements relating to the MHRA, FDA & EMA regulations. A thorough understanding of CGMP requirements is also essential. Significant pharmaceutical compliance and a comprehensive understanding of Regulatory requirements are essentialThis is a permanent position based in Queenborough, Kent. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • maidenhead, south east
      • temporary
      • randstad inhouse services
      Randstad are looking for a Graduate Technical Service Specialist to work across a number of sites and laboratories across the UK. The Technical Service Specialist is responsible for performing planned maintenance activities, hardware and software upgrades and for back up first level one service and assisting with installations and deinstallations.Responsibilities:Provide first line service to the client Schedule and perform planned maintenance (PM activities)Assist with instrument installations and deinstallationsSuccess in this role is measured by customer satisfaction score, service key performance indicators achievement and economic growth and profitability per district Background:Proven track record in a similar position supported by management and customer referencesSuccessful engagement with customers, specifically lab staffTechnical expert for product line responsibilityStrong communication skillsAbility to identify and drive resolution of issuesString experience of use of analytical tools and software
      Randstad are looking for a Graduate Technical Service Specialist to work across a number of sites and laboratories across the UK. The Technical Service Specialist is responsible for performing planned maintenance activities, hardware and software upgrades and for back up first level one service and assisting with installations and deinstallations.Responsibilities:Provide first line service to the client Schedule and perform planned maintenance (PM activities)Assist with instrument installations and deinstallationsSuccess in this role is measured by customer satisfaction score, service key performance indicators achievement and economic growth and profitability per district Background:Proven track record in a similar position supported by management and customer referencesSuccessful engagement with customers, specifically lab staffTechnical expert for product line responsibilityStrong communication skillsAbility to identify and drive resolution of issuesString experience of use of analytical tools and software
      • queenborough, south east
      • permanent
      • £20,000 - £25,000 per year
      • randstad cpe
      My client, a specialist Pharma manufacturing business has an exciting role for a Senior Analyst to join their microbiology team.As Microbiology Analyst, you will perform microbiology testing on non-sterile raw materials, intermediates and finished products and work on site-wide environmental monitoring programmes.As Microbiology Analyst, you will:Verify laboratory data and ensure accurate primary records are kept.Develop a training plan in conjunction with laboratory trainers and Team Leader. Perform training where appropriateUndertake projects, impact goals and specific responsibilities as required by Laboratories.To be considered for the role of Microbiology Analyst, you will:Biological Science degree qualified or equivalentQC Microbiology laboratory experienceExperience in training and managing laboratory staffThis is a Permanent position, based in Queenborough. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      My client, a specialist Pharma manufacturing business has an exciting role for a Senior Analyst to join their microbiology team.As Microbiology Analyst, you will perform microbiology testing on non-sterile raw materials, intermediates and finished products and work on site-wide environmental monitoring programmes.As Microbiology Analyst, you will:Verify laboratory data and ensure accurate primary records are kept.Develop a training plan in conjunction with laboratory trainers and Team Leader. Perform training where appropriateUndertake projects, impact goals and specific responsibilities as required by Laboratories.To be considered for the role of Microbiology Analyst, you will:Biological Science degree qualified or equivalentQC Microbiology laboratory experienceExperience in training and managing laboratory staffThis is a Permanent position, based in Queenborough. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
      • maidenhead, south east
      • temporary
      • £12.50 per hour
      • randstad inhouse services
      Are you looking for a part time role a few days per week? Are you looking to support essential workers? If yes, we have a fantastic opportunity for you. On behalf of our client we are recruiting for a number of COVID-19 Rapid Test Operatives to support the implementation and delivery of the Rapid Covid-19 testing programme based on our client's site. Benefits You'll Love:Training and full personal protective equipment providedFree on-site parking Subsidised onsite canteen Outside seating areasPay Rate & Hours:Wednesday: 08:30am - 16:30pm and Thursday: 09.00am - 15.30pm £12.50 per hourResponsibilities: Administer rapid throat and nasal swab tests on a daily basis Delivery of testing servicesReport on test results Following on site health and safety Requirements:Not be classified or live with anyone in the COVID-19 high risk groups Good interpersonal skills Data entry experience IT proficient Eligible to live and work in the UKOver 18 1 year of referencing (employment or alternative activity) Desirable:Experience in a medical, clinical or health setting If you tick all the boxes, then why not click apply today!
      Are you looking for a part time role a few days per week? Are you looking to support essential workers? If yes, we have a fantastic opportunity for you. On behalf of our client we are recruiting for a number of COVID-19 Rapid Test Operatives to support the implementation and delivery of the Rapid Covid-19 testing programme based on our client's site. Benefits You'll Love:Training and full personal protective equipment providedFree on-site parking Subsidised onsite canteen Outside seating areasPay Rate & Hours:Wednesday: 08:30am - 16:30pm and Thursday: 09.00am - 15.30pm £12.50 per hourResponsibilities: Administer rapid throat and nasal swab tests on a daily basis Delivery of testing servicesReport on test results Following on site health and safety Requirements:Not be classified or live with anyone in the COVID-19 high risk groups Good interpersonal skills Data entry experience IT proficient Eligible to live and work in the UKOver 18 1 year of referencing (employment or alternative activity) Desirable:Experience in a medical, clinical or health setting If you tick all the boxes, then why not click apply today!

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