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    17 Contract Pharmaceutical found

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      • maidenhead, south east
      • contract
      Are you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to und
      Are you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to und
      • reading, south east
      • contract
      • £15.00 - £20.00 per hour
      Job Title: Junior Team Leader - MicrobiologyLocation: ReadingDuration: Until 2nd December 2025Pay Rate: £20 an hourJob Overview:Working as part of a cross-functional team at client, you will deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience. You will also hold accountability and responsibility for the testing team, providing
      Job Title: Junior Team Leader - MicrobiologyLocation: ReadingDuration: Until 2nd December 2025Pay Rate: £20 an hourJob Overview:Working as part of a cross-functional team at client, you will deliver the RDQ activities required to complete new product development, portfolio maintenance and/or productivity projects with an emphasis on meeting the desired consumer experience. You will also hold accountability and responsibility for the testing team, providing
      • witney, south east
      • contract
      Are you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to und
      Are you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to und
      • offaly, international
      • contract
      • €42,000 - €45,000 per year
      ResponsibilitiesEnsure training documentation is current and accessible; support overall LMS functionality.Coordinate issuance and reconciliation of documents and labels to meet production and project timelines.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global t
      ResponsibilitiesEnsure training documentation is current and accessible; support overall LMS functionality.Coordinate issuance and reconciliation of documents and labels to meet production and project timelines.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global t
      • maidenhead, south east
      • contract
      Are you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of our clients regulatory project team representing Middle East Africa, Turkey, CIS & Russia and Central Eastern European Markets in the International Growth Markets team with accountability for 1-3 products progressing through NDA planning, filing and app
      Are you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of our clients regulatory project team representing Middle East Africa, Turkey, CIS & Russia and Central Eastern European Markets in the International Growth Markets team with accountability for 1-3 products progressing through NDA planning, filing and app
      • maidenhead, south east
      • contract
      Are you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of the Global Regulatory Project team representing the international Growth markets with accountability for 1-3 marketed products across APAC, MART CEER and LatAm. You will be developing and implementing regulatory strategies to support product lifecycle ma
      Are you an experienced Senior Regulatory Affairs Manager? Do you have experience in the International Growth Markets? If so, we would love to hear from you! The successful candidate will become a member of the Global Regulatory Project team representing the international Growth markets with accountability for 1-3 marketed products across APAC, MART CEER and LatAm. You will be developing and implementing regulatory strategies to support product lifecycle ma
      • wakefield, yorkshire and the humber
      • contract
      • £12.94 per hour
      Do you have a passion for making a positive impact on the environment and the lives of others? As a QESH Coordinator, you will play a vital role in ensuring our operations comply with all relevant regulations and standards. Our client manufactures, distributes, sells and markets some of the world's strongest brands in non-alcoholic beverages. It is a leading Western European marketer, distributor, and producer of bottles and can non-alcoholic refreshment.
      Do you have a passion for making a positive impact on the environment and the lives of others? As a QESH Coordinator, you will play a vital role in ensuring our operations comply with all relevant regulations and standards. Our client manufactures, distributes, sells and markets some of the world's strongest brands in non-alcoholic beverages. It is a leading Western European marketer, distributor, and producer of bottles and can non-alcoholic refreshment.
      • slough, south east
      • contract
      Are you experienced in the Health, Safety, and Environmental space? Are you NEBOSH / IOSH qualified? Our Biotechnology client is looking for a proactive and experienced HSE Advisor to join their team, supporting their business move to a brand new state-of-the-art facility! This is a contract position, offered initially for 12 months, but anticipated to last 2 years due to the length of the project. The successful candidate will play a role in ensuring the
      Are you experienced in the Health, Safety, and Environmental space? Are you NEBOSH / IOSH qualified? Our Biotechnology client is looking for a proactive and experienced HSE Advisor to join their team, supporting their business move to a brand new state-of-the-art facility! This is a contract position, offered initially for 12 months, but anticipated to last 2 years due to the length of the project. The successful candidate will play a role in ensuring the
      • maidenhead, south east
      • contract
      Are you an experienced Senior Pharmacovigilance Scientist? Are you interested in overseeing and leading the process for safety signal management activities and aggregate reports? If so, we would love to speak with you. We are hiring for a Senior PV Scientist to join a globally leading Biotechnology client of ours, ensuring products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies are
      Are you an experienced Senior Pharmacovigilance Scientist? Are you interested in overseeing and leading the process for safety signal management activities and aggregate reports? If so, we would love to speak with you. We are hiring for a Senior PV Scientist to join a globally leading Biotechnology client of ours, ensuring products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies are
      • city of manchester, north west
      • contract
      Are you an experienced Medical Science Liaison Manager? Are you strong in delivering field-led projects, collaborating with cross-functional field and therapy area teams, and a high focus on scientific exchange/customer engagement and relationships? If so, we would love to speak with you! We are recruiting for a Medical Science Liaison Manager (or senior level depending on experience) to join our globally leading Biotechnology client. The successful candid
      Are you an experienced Medical Science Liaison Manager? Are you strong in delivering field-led projects, collaborating with cross-functional field and therapy area teams, and a high focus on scientific exchange/customer engagement and relationships? If so, we would love to speak with you! We are recruiting for a Medical Science Liaison Manager (or senior level depending on experience) to join our globally leading Biotechnology client. The successful candid
      • melton mowbray, east midlands
      • contract
      Are you an experienced Research Technician? Do you have strong practical knowledge of animal behaviour and experience in research study implementation? If so, we would love to speak with you! We are hiring for a Research Technician to join our clients Applied Behaviour R&D Team to play a crucial role in conducting research trials, collecting high-quality behavioural data, and supporting scientific advancements in our clients brands globally. The role requi
      Are you an experienced Research Technician? Do you have strong practical knowledge of animal behaviour and experience in research study implementation? If so, we would love to speak with you! We are hiring for a Research Technician to join our clients Applied Behaviour R&D Team to play a crucial role in conducting research trials, collecting high-quality behavioural data, and supporting scientific advancements in our clients brands globally. The role requi
      • maidenhead, south east
      • contract
      Are you an experienced Medical Information Manager? Do you have experience working with third party Medical Information providers? If so, we would love to hear from you! The successful candidate will be responsible for leading the Medical Information function and managing Medical Information activity. The individual will need to provide oversight of our clients third-party medical information agency, develop responses to second line enquiries, develop stan
      Are you an experienced Medical Information Manager? Do you have experience working with third party Medical Information providers? If so, we would love to hear from you! The successful candidate will be responsible for leading the Medical Information function and managing Medical Information activity. The individual will need to provide oversight of our clients third-party medical information agency, develop responses to second line enquiries, develop stan
      • slough, south east
      • contract
      Do you want to help shape the delivery of next generation antibody therapeutics? Do you have knowledge of molecular biology and microbiological methods, and a proven track record of antibody discovery or protein engineering? If so, we would love to hear from you! We are recruiting for an Antibody Discovery and Engineering Scientist, at either Senior or Research Scientist level. This role is offered on a contract basis initially for 12 months. This is an ex
      Do you want to help shape the delivery of next generation antibody therapeutics? Do you have knowledge of molecular biology and microbiological methods, and a proven track record of antibody discovery or protein engineering? If so, we would love to hear from you! We are recruiting for an Antibody Discovery and Engineering Scientist, at either Senior or Research Scientist level. This role is offered on a contract basis initially for 12 months. This is an ex
      • reading, south east
      • contract
      • £18.00 - £20.00 per hour
      Are you an experienced Microbiology scientist? Have a lead a small group of people within laboratory as a lead scientist? We have an opportunity for you for a Microbiology Lead Scientist Role: Microbiology Lead ScientistLocation: ReadingShifts: Thursday - Monday, 09:00 - 05:00 Work Model: Fully on-siteJob type: ContractSalary: £20 p/hJob overviewWorking as part of a cross-functional team, you will deliver the RDQ activities required to complete new product
      Are you an experienced Microbiology scientist? Have a lead a small group of people within laboratory as a lead scientist? We have an opportunity for you for a Microbiology Lead Scientist Role: Microbiology Lead ScientistLocation: ReadingShifts: Thursday - Monday, 09:00 - 05:00 Work Model: Fully on-siteJob type: ContractSalary: £20 p/hJob overviewWorking as part of a cross-functional team, you will deliver the RDQ activities required to complete new product
      • tullamore, international
      • contract
      • €60,000 - €67,000 per year
      Our Global Pharmaceuticals client is currently hiring for a Environmental, Health and Safety Specialist position. Responsible for the ongoing development of the EHS management system and it's component parts, (SOPs, Training documents and policies) to ensure regulatory and corporate compliance. Ensure compliance with applicable regulatory and corporate health and safety requirements in a manner consistent with continued plant profitability. This is a contr
      Our Global Pharmaceuticals client is currently hiring for a Environmental, Health and Safety Specialist position. Responsible for the ongoing development of the EHS management system and it's component parts, (SOPs, Training documents and policies) to ensure regulatory and corporate compliance. Ensure compliance with applicable regulatory and corporate health and safety requirements in a manner consistent with continued plant profitability. This is a contr
      • witney, south east
      • contract
      Are you passionate about science and enjoy working in a fast-paced laboratory environment?Do you thrive in a detail-oriented role and have a knack for organisation?If so, we're looking for you! We are seeking a highly motivated R&D Laboratory Technician to join our team at a leading global medical device and health care company based in Witney, Oxfordshire. You will play a crucial role in supporting our R&D sensor laboratory team, ensuring the smooth opera
      Are you passionate about science and enjoy working in a fast-paced laboratory environment?Do you thrive in a detail-oriented role and have a knack for organisation?If so, we're looking for you! We are seeking a highly motivated R&D Laboratory Technician to join our team at a leading global medical device and health care company based in Witney, Oxfordshire. You will play a crucial role in supporting our R&D sensor laboratory team, ensuring the smooth opera
      • didcot, south east
      • contract
      Do you thrive in a fast-paced, regulated environment and have a passion for detail?This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.As the QA Admin - Document Control & Training, you will:Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, mainte
      Do you thrive in a fast-paced, regulated environment and have a passion for detail?This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.As the QA Admin - Document Control & Training, you will:Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, mainte

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