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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.
      • 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.
      • dundee, scotland
      • contract
      • £15.00 - £18.80 per hour
      • randstad cpe
      My client, a medical device business has an exciting requirement for a Validation Engineer to join their site in Dundee on a 12 Month contract. Responsibilities include:* Prepare and manage validation activities, including document approval and protocol implementation.* Author validation documentation including, but not limited to, Installation, Operational and Performance Qualification protocols and reports, Process Validation protocols and reports, and Protocol Discrepancies and Addenda; IQ/OQ/PQ.* Ensure Standard operating procedures are adhered to in relation to current regulatory requirements/guidelines.* Create reports surrounding progression and escalating any issues effectively.* Keep current on regulatory and quality requirements for regulated testing, qualification, and validation activities.Requirements:* Degree level qualification in engineering or relevant scientific discipline.* Ideally a minimum of 1 year industry experience within medical devices. Although, this is not essential.* Experience of drafting and executing validation protocols and reports.* High attention to detail.* Excellent problem solving skills.12 Month PAYE contract. 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 medical device business has an exciting requirement for a Validation Engineer to join their site in Dundee on a 12 Month contract. Responsibilities include:* Prepare and manage validation activities, including document approval and protocol implementation.* Author validation documentation including, but not limited to, Installation, Operational and Performance Qualification protocols and reports, Process Validation protocols and reports, and Protocol Discrepancies and Addenda; IQ/OQ/PQ.* Ensure Standard operating procedures are adhered to in relation to current regulatory requirements/guidelines.* Create reports surrounding progression and escalating any issues effectively.* Keep current on regulatory and quality requirements for regulated testing, qualification, and validation activities.Requirements:* Degree level qualification in engineering or relevant scientific discipline.* Ideally a minimum of 1 year industry experience within medical devices. Although, this is not essential.* Experience of drafting and executing validation protocols and reports.* High attention to detail.* Excellent problem solving skills.12 Month PAYE contract. 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.
      • dundee, scotland
      • contract
      • randstad cpe
      Do you have a scientific background with an understanding of process validation principles and procedures? Are you comfortable working as an individual and as part of a team? We are looking for a Manufacturing Scientist to join a pioneering organisation focused on the development and manufacturing of important and innovative in vitro diagnostic tests for use in clinical laboratories.The successful candidate will be working in a technical operations environment, the Manufacturing Scientist will be responsible for safely ensuring the on-time production of materials which conform to current best practices and quality standards, and is aligned to the expectations set by the Product Leads. This role is offered on a contract basis, initially for 5 months with the potential for extension. We have multiple roles available, across various shifts: M-F 8am-4pm or 4pm-12am. Responsibilities:Conducting all activities in accordance with the Health & Safety culture. Enthusiastically assuming responsibility for personal workload.Planning and coordinating all aspects of personal workload for specified job assignments, e.g. raw material testing, bulk reagent production, in-process testing, QC release testing, protein purifications, high-performance liquid chromatography (HPLC), etc. Performing Enterprise Resource Planning (ERP) transactions as part of works order management.Work with peers and colleagues to ensure on-time delivery of the production schedule which meets all requirements of both internal and external customers.Working to develop in-depth understanding of products, processes and procedures.Taking full accountability for personal workload, ensuring quality documentation is completed to a high standard and mistakes are rectified in a timely manner. Proactively contributing to continuous improvement initiatives and other general housekeeping duties.Taking a self-motivated approach to continuous professional development and engaging with site training initiatives/requirements. Developing excellent relations with the department team and wider Operations group. Proposing ideas for new opportunities to improve communication and productivity.Leveraging skills and experience, providing local leadership, coaching and mentoring to peers and colleagues in the Technical Operations group.Being aware of the policies as set out in the Dundee Employee Handbook and able to enact them as appropriate.Qualifications: Undergraduate/bachelor's degree in Life Sciences, Biological Sciences or Chemical Sciences.Background: A demonstrable technical understanding of the function and performance characteristics of the products and materials produced within the Technical Operations environment.A detailed knowledge of production process control procedures and best practices.An ability to navigate Electronic Document Management Systems (EDMS) and execute document control procedures. An understanding of and ability to apply Statistical Process Control (SPC) techniques, including generating trend reports.A basic appreciation for Enterprise Resource Planning (ERP) costs and how to influence them.An understanding of Corrective and preventative Action (CAPA) and Change Control principles with the ability to process records within the respective databases/systems.An ability to employ state-of-the-art Root Cause Analysis (RCA) tools, including A3/DMAIC.An understanding of and ability to contribute to Risk Assessment activities, Risk Management/Control exercises, and Failure Mode Effect Analyses (FMEA).An understanding of Process Validation principles and procedures with the ability to execute. 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 a scientific background with an understanding of process validation principles and procedures? Are you comfortable working as an individual and as part of a team? We are looking for a Manufacturing Scientist to join a pioneering organisation focused on the development and manufacturing of important and innovative in vitro diagnostic tests for use in clinical laboratories.The successful candidate will be working in a technical operations environment, the Manufacturing Scientist will be responsible for safely ensuring the on-time production of materials which conform to current best practices and quality standards, and is aligned to the expectations set by the Product Leads. This role is offered on a contract basis, initially for 5 months with the potential for extension. We have multiple roles available, across various shifts: M-F 8am-4pm or 4pm-12am. Responsibilities:Conducting all activities in accordance with the Health & Safety culture. Enthusiastically assuming responsibility for personal workload.Planning and coordinating all aspects of personal workload for specified job assignments, e.g. raw material testing, bulk reagent production, in-process testing, QC release testing, protein purifications, high-performance liquid chromatography (HPLC), etc. Performing Enterprise Resource Planning (ERP) transactions as part of works order management.Work with peers and colleagues to ensure on-time delivery of the production schedule which meets all requirements of both internal and external customers.Working to develop in-depth understanding of products, processes and procedures.Taking full accountability for personal workload, ensuring quality documentation is completed to a high standard and mistakes are rectified in a timely manner. Proactively contributing to continuous improvement initiatives and other general housekeeping duties.Taking a self-motivated approach to continuous professional development and engaging with site training initiatives/requirements. Developing excellent relations with the department team and wider Operations group. Proposing ideas for new opportunities to improve communication and productivity.Leveraging skills and experience, providing local leadership, coaching and mentoring to peers and colleagues in the Technical Operations group.Being aware of the policies as set out in the Dundee Employee Handbook and able to enact them as appropriate.Qualifications: Undergraduate/bachelor's degree in Life Sciences, Biological Sciences or Chemical Sciences.Background: A demonstrable technical understanding of the function and performance characteristics of the products and materials produced within the Technical Operations environment.A detailed knowledge of production process control procedures and best practices.An ability to navigate Electronic Document Management Systems (EDMS) and execute document control procedures. An understanding of and ability to apply Statistical Process Control (SPC) techniques, including generating trend reports.A basic appreciation for Enterprise Resource Planning (ERP) costs and how to influence them.An understanding of Corrective and preventative Action (CAPA) and Change Control principles with the ability to process records within the respective databases/systems.An ability to employ state-of-the-art Root Cause Analysis (RCA) tools, including A3/DMAIC.An understanding of and ability to contribute to Risk Assessment activities, Risk Management/Control exercises, and Failure Mode Effect Analyses (FMEA).An understanding of Process Validation principles and procedures with the ability to execute. 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.
      • 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.
      • 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.

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