Thank you for subscribing to your personalised job alerts.

    4 jobs found for quality

    filter3
    clear all
      • maidenhead, south east
      • temporary
      • £30.00 - £40.00 per hour
      • randstad business support
      JOB TITLE: Quality Assurance & Regulatory Compliance Manager - North EuropeSTART DATE: ASAPEND DATE: 6 Months Contract (Potential Perm)PAY RATE: £30 - £40 Per HourLOCATION: Maidenhead (Office based - Open to flexible) The ClientSpecialising in the emerging market of diagnostics agents , our client is a global health care leader that has a large product area in Diabetes, Arthritis, Sepsis, Pregnancy and many more. The biggest regions that they are working within are in Africa, Asia, Latin America and Eastern Europe. Corona virus has been a massive growth engine for all departments further enhancing portfolios of life-changing technologies. The ProjectWith product development a key component for the team, project management combined with Quality Assurance and Regulatory Compliance is key. The department works closely with their Northern European counterparts on a daily basis to develop new products as well as improving existing products. This involves an ongoing process of establishing and maintaining quality systems within different regional levels. The CandidateThe ideal candidate would be someone who has experience in managing and dealing within multiple projects within a regulated market. They must be able to prioritise tasks to meet the company's milestone with key attention to detail. Furthermore, the ideal candidate must have experience in the implantable medical device industry. However, we would be open to candidates who have experience within the airline industry. What we are looking for:Educated to degree level or with equivalent relevant experienceExperience of medical device regulationsPrevious experience in the implantable medical device industry is preferred.Knowledge of ISO 13485, ISO 9000 and/or ISO 14001 desirable.Analytical, detail oriented. Good organising, planning, verbal and written skills.Strong interpersonal skills, with the ability to build and maintain relationshipsComfortable in a matrix environment and interfacing with different international sites and business units Full Job description will be provided for applicants.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      JOB TITLE: Quality Assurance & Regulatory Compliance Manager - North EuropeSTART DATE: ASAPEND DATE: 6 Months Contract (Potential Perm)PAY RATE: £30 - £40 Per HourLOCATION: Maidenhead (Office based - Open to flexible) The ClientSpecialising in the emerging market of diagnostics agents , our client is a global health care leader that has a large product area in Diabetes, Arthritis, Sepsis, Pregnancy and many more. The biggest regions that they are working within are in Africa, Asia, Latin America and Eastern Europe. Corona virus has been a massive growth engine for all departments further enhancing portfolios of life-changing technologies. The ProjectWith product development a key component for the team, project management combined with Quality Assurance and Regulatory Compliance is key. The department works closely with their Northern European counterparts on a daily basis to develop new products as well as improving existing products. This involves an ongoing process of establishing and maintaining quality systems within different regional levels. The CandidateThe ideal candidate would be someone who has experience in managing and dealing within multiple projects within a regulated market. They must be able to prioritise tasks to meet the company's milestone with key attention to detail. Furthermore, the ideal candidate must have experience in the implantable medical device industry. However, we would be open to candidates who have experience within the airline industry. What we are looking for:Educated to degree level or with equivalent relevant experienceExperience of medical device regulationsPrevious experience in the implantable medical device industry is preferred.Knowledge of ISO 13485, ISO 9000 and/or ISO 14001 desirable.Analytical, detail oriented. Good organising, planning, verbal and written skills.Strong interpersonal skills, with the ability to build and maintain relationshipsComfortable in a matrix environment and interfacing with different international sites and business units Full Job description will be provided for applicants.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
      • tullamore, international
      • permanent
      • randstad financial services
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D. Site Compliance and Product Release Senior Specialist / Qualified PersonThe Site Compliance and Product Release Senior Specialist / Qualified Person will have an active role in batch review and certification for batches manufactured on site as well as partaking in batch review and certification of outsourced manufacturing & testing activities. Duties & ResponsibilitiesSupport the implementation & continuous improvement of an effective quality management system including quality oversight across the site.Assume an active role in the creation, modification and maintenance of the Quality Management Systems supporting operational and release functions.Review & approval of batch records and associated raw data for manufacturing operations to ensure compliance with the requirements of cGMP and batch review and batch disposition process.Participate in and support Site License registration process and future license updates.Review of analytical data and associated reports.Review and approval of non-conformance events and reports including deviations, laboratory investigations & environmental excursions.Perform batch review and approval of investigational products and commercial products.Participate in or lead internal and external audit including 3rd party audits and supplier reviews.Interface with other departments such as Engineering, Laboratories, Operations, Warehouse and Process Development to ensure quality objectives are understood and achieved.Initiate and implement change control activities in accordance with site procedures.Assist with oversight of issue management and non-conformance events to ensure compliance and timely closure.Maintains a contemporary understanding of cGMP regulations and guidance in relation to all aspects of validation across manufacturing, laboratories and facilities.Partake in or lead periodic quality review meetings to ensure compliance and continuous improvement.Write or assist in writing, reviewing and approval of SOPs and other GMP documents. Qualifications and ExperienceBSc, MSC in a relevant discipline (e.g biochemistry, chemistry, process engineering) and be QP qualified.At least 4-7 years relevant experience in a Pharma (Sterile) /BioPharma Manufacturing environment.Biotech/Pharmaceutical QA experience with a strong knowledge of cGMP.Experience of interaction with cross functional departments.Good knowledge of regulatory and cGMP guidelines and directives, including product certification, validation, quality control and manufacture including QbD and Risk Management.Ability to support relevant sections of CTD for regulatory submission.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      Why work for this company?Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries. Company Profile65+ years of experience in animal health.Nearly $6 billion annual revenues.25 manufacturing sites around the world.10,000 employees worldwide of which 1,100 employees are committed to R&D. Site Compliance and Product Release Senior Specialist / Qualified PersonThe Site Compliance and Product Release Senior Specialist / Qualified Person will have an active role in batch review and certification for batches manufactured on site as well as partaking in batch review and certification of outsourced manufacturing & testing activities. Duties & ResponsibilitiesSupport the implementation & continuous improvement of an effective quality management system including quality oversight across the site.Assume an active role in the creation, modification and maintenance of the Quality Management Systems supporting operational and release functions.Review & approval of batch records and associated raw data for manufacturing operations to ensure compliance with the requirements of cGMP and batch review and batch disposition process.Participate in and support Site License registration process and future license updates.Review of analytical data and associated reports.Review and approval of non-conformance events and reports including deviations, laboratory investigations & environmental excursions.Perform batch review and approval of investigational products and commercial products.Participate in or lead internal and external audit including 3rd party audits and supplier reviews.Interface with other departments such as Engineering, Laboratories, Operations, Warehouse and Process Development to ensure quality objectives are understood and achieved.Initiate and implement change control activities in accordance with site procedures.Assist with oversight of issue management and non-conformance events to ensure compliance and timely closure.Maintains a contemporary understanding of cGMP regulations and guidance in relation to all aspects of validation across manufacturing, laboratories and facilities.Partake in or lead periodic quality review meetings to ensure compliance and continuous improvement.Write or assist in writing, reviewing and approval of SOPs and other GMP documents. Qualifications and ExperienceBSc, MSC in a relevant discipline (e.g biochemistry, chemistry, process engineering) and be QP qualified.At least 4-7 years relevant experience in a Pharma (Sterile) /BioPharma Manufacturing environment.Biotech/Pharmaceutical QA experience with a strong knowledge of cGMP.Experience of interaction with cross functional departments.Good knowledge of regulatory and cGMP guidelines and directives, including product certification, validation, quality control and manufacture including QbD and Risk Management.Ability to support relevant sections of CTD for regulatory submission.Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003
      • chelmsford, east of england
      • temporary
      • £9.50 - £11.81 per hour
      • randstad business support
      Laboratory Analyst Chelmsford£9.50 per hour6 weeks temporary position37 hours per weekAre you interested in science and looking for your next role? Are you pro-active and enjoy working in a close-knit environment? If so, read on.A well known utilities organisation based in Chelmsford are looking for a Laboratory Analyst to join them for 6 weeks on a temporary basis.The Benefits:*Working for an established Water Company*Friendly team*Holiday Pay*Pension schemeThe Duties:* Process samples and/or media in accordance with our documented methods and procedures* Quality compliance* Provide polite efficient service to customers and colleagues* Ongoing competency and CPD* Maintain Health and safety standardsRequirements: Experience working within a laboratory environment - 3 months essentialAble to demonstrate competency in all basic laboratory techniquesMinimum Level 2 i.e.5 GCSEs to include a scientific discipline (with potential to study BTEC or equivalent)Please note, due to the location of this office, you will need to drive and have access to a vehicle.We are looking to get a member of staff in this post as soon as possible, please apply today if this is the role for you.Randstad Business Support acts as an employment business when supplying temporary staff and as an employment agency when introducing candidates for permanent employment with a client. Randstad Business Support is an equal opportunities employer and decisions are made on merits alone.
      Laboratory Analyst Chelmsford£9.50 per hour6 weeks temporary position37 hours per weekAre you interested in science and looking for your next role? Are you pro-active and enjoy working in a close-knit environment? If so, read on.A well known utilities organisation based in Chelmsford are looking for a Laboratory Analyst to join them for 6 weeks on a temporary basis.The Benefits:*Working for an established Water Company*Friendly team*Holiday Pay*Pension schemeThe Duties:* Process samples and/or media in accordance with our documented methods and procedures* Quality compliance* Provide polite efficient service to customers and colleagues* Ongoing competency and CPD* Maintain Health and safety standardsRequirements: Experience working within a laboratory environment - 3 months essentialAble to demonstrate competency in all basic laboratory techniquesMinimum Level 2 i.e.5 GCSEs to include a scientific discipline (with potential to study BTEC or equivalent)Please note, due to the location of this office, you will need to drive and have access to a vehicle.We are looking to get a member of staff in this post as soon as possible, please apply today if this is the role for you.Randstad Business Support acts as an employment business when supplying temporary staff and as an employment agency when introducing candidates for permanent employment with a client. Randstad Business Support is an equal opportunities employer and decisions are made on merits alone.
      • loughton, east of england
      • temp to perm
      • randstad inhouse services
      Radstad are working with a leading healthcare provider to revruit a Customer Service Specialistis part of a 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 Customer Service Specialist is within our Rapid Diagnostics business working across the UK. This role requires you to work in line with the standard operating procedures whilst ensuring all KPI's are achieved. The work you perform as part of this role, impacts on our customer experience and will assist to maximise the operational efficiencyand effectiveness of Customer Operations.As an enthusiastic organised individual with good attention to detail you will work together with the other administrators in the results team to ensure that all information following occupational health and drug and alcohol appointments is recorded accurately and that results are dispatched to the customer in a timely manner within the agreed SLA. You will have a cheerful professional phone manner and feel comfortable dealing withcustomer enquiries.A flexible approach to work will enable you to adapt to changing priorities within the teamand support colleagues from within the team or wider business to ensure that the customerreceives the highest level of service at all times.RESPONSIBILITIES:You are responsible for providing support in customer service functions in order to continueto provide our customers with the very best service possible. To achieve this you will beexpected to- Work methodically to ensure that standard operating procedures are followed and that workload is prioritised appropriately to meet agreed SLA's / KPI's- Acurately complete all tasks performed which may include but are not limited to;- Work methodically to ensure that the standard operating procedures are followed and that the workload is prioritised appropriately and meets agreed SLA's- Use reports and dashboards to ensure that all available paperwork and results are allocated appropriately and that there are no cases on the outstanding list at the end of each day- Upload results to the Sentinel Database- Liaise with Occupational Health Physicians to obtain fit slips and reports following appointments, following up on the progress of cases where further information is required to complete the case- Ensure that the review and reporting of results is performed in a timely manner within SLA- Ensure that all paperwork is uploaded on to the system, data entered accurately and information allocated correctly. Regularly following up on outstandinginformation which is preventing a case from being closed- Diligently answer queries from customers via telephone and email, answering the customer services phone line within 3 rings- Participate in complaint investigation and audits as and when required- Ensure standard operating procedures remain up to date- Proactively contribute to process improvements, suggesting ideas which would benefit the efficiency of your team- You should understand the Key Performance Indicators (KPIs) which directly relate to your team performance and identify ways of improving performance against these targets BASIC QUALIFICATIONS | EDUCATION:- Previous experience within an administrative or customer service role- Excellent verbal, written and communication skills- A dynamic team player who is collaborative but leads by example- IT literate with a good level of experience in Word, Excel & OutlookPREFERRED QUALIFICATIONS:- Proven experience in an administrative or customer service positionCOMPETENCIES:- Achieve - Be a role model and instilling the values of the organisation, driving the understanding and importance of good customer service in the overall delivery of service to the customer- Grow - Complete tasks and other ad-hoc projects that may arise as directed by your Supervisor / Manager- Engage - You will be required to communicate with other members of your team to ensure work is completed and prioritized accordingly- Develops Talent - Be innovative and suggest ways to help us improve and develop- Drives for Results- Monitor and manage changes to demonstrate improvements in KPI's or performance related issues- Focuses on Customers- You will be customer focused with previous experience in working in a busy team.
      Radstad are working with a leading healthcare provider to revruit a Customer Service Specialistis part of a 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 Customer Service Specialist is within our Rapid Diagnostics business working across the UK. This role requires you to work in line with the standard operating procedures whilst ensuring all KPI's are achieved. The work you perform as part of this role, impacts on our customer experience and will assist to maximise the operational efficiencyand effectiveness of Customer Operations.As an enthusiastic organised individual with good attention to detail you will work together with the other administrators in the results team to ensure that all information following occupational health and drug and alcohol appointments is recorded accurately and that results are dispatched to the customer in a timely manner within the agreed SLA. You will have a cheerful professional phone manner and feel comfortable dealing withcustomer enquiries.A flexible approach to work will enable you to adapt to changing priorities within the teamand support colleagues from within the team or wider business to ensure that the customerreceives the highest level of service at all times.RESPONSIBILITIES:You are responsible for providing support in customer service functions in order to continueto provide our customers with the very best service possible. To achieve this you will beexpected to- Work methodically to ensure that standard operating procedures are followed and that workload is prioritised appropriately to meet agreed SLA's / KPI's- Acurately complete all tasks performed which may include but are not limited to;- Work methodically to ensure that the standard operating procedures are followed and that the workload is prioritised appropriately and meets agreed SLA's- Use reports and dashboards to ensure that all available paperwork and results are allocated appropriately and that there are no cases on the outstanding list at the end of each day- Upload results to the Sentinel Database- Liaise with Occupational Health Physicians to obtain fit slips and reports following appointments, following up on the progress of cases where further information is required to complete the case- Ensure that the review and reporting of results is performed in a timely manner within SLA- Ensure that all paperwork is uploaded on to the system, data entered accurately and information allocated correctly. Regularly following up on outstandinginformation which is preventing a case from being closed- Diligently answer queries from customers via telephone and email, answering the customer services phone line within 3 rings- Participate in complaint investigation and audits as and when required- Ensure standard operating procedures remain up to date- Proactively contribute to process improvements, suggesting ideas which would benefit the efficiency of your team- You should understand the Key Performance Indicators (KPIs) which directly relate to your team performance and identify ways of improving performance against these targets BASIC QUALIFICATIONS | EDUCATION:- Previous experience within an administrative or customer service role- Excellent verbal, written and communication skills- A dynamic team player who is collaborative but leads by example- IT literate with a good level of experience in Word, Excel & OutlookPREFERRED QUALIFICATIONS:- Proven experience in an administrative or customer service positionCOMPETENCIES:- Achieve - Be a role model and instilling the values of the organisation, driving the understanding and importance of good customer service in the overall delivery of service to the customer- Grow - Complete tasks and other ad-hoc projects that may arise as directed by your Supervisor / Manager- Engage - You will be required to communicate with other members of your team to ensure work is completed and prioritized accordingly- Develops Talent - Be innovative and suggest ways to help us improve and develop- Drives for Results- Monitor and manage changes to demonstrate improvements in KPI's or performance related issues- Focuses on Customers- You will be customer focused with previous experience in working in a busy team.

    Thank you for subscribing to your personalised job alerts.

    It looks like you want to switch your language. This will reset your filters on your current job search.