Complaints Investigator - Witney, Oxfordshire (Night Shift)Are you a meticulous problem-solver with an analytical mind? Do you want to contribute to the quality and safety of essential medical devices? We're looking for a Complaints Investigator to join our team at a leading global medical device and health care company in Witney, Oxfordshire. This is a fantastic opportunity to kick-start your career in a vital role, with full training provided - no prior
Complaints Investigator - Witney, Oxfordshire (Night Shift)Are you a meticulous problem-solver with an analytical mind? Do you want to contribute to the quality and safety of essential medical devices? We're looking for a Complaints Investigator to join our team at a leading global medical device and health care company in Witney, Oxfordshire. This is a fantastic opportunity to kick-start your career in a vital role, with full training provided - no prior
ResponsibilitiesPerform routine and non-routine microbiological testing with accurate documentation.Manage lab operations: scheduling, equipment, stock control, and maintenance.Ensure a safe, compliant lab environment aligned with SOPs and quality standards.Maintain quality systems (cGLP), including SOPs, validations, investigations, and trend reviews.Collaborate cross-functionally to support projects and continuous improvement.Lead contamination control e
ResponsibilitiesPerform routine and non-routine microbiological testing with accurate documentation.Manage lab operations: scheduling, equipment, stock control, and maintenance.Ensure a safe, compliant lab environment aligned with SOPs and quality standards.Maintain quality systems (cGLP), including SOPs, validations, investigations, and trend reviews.Collaborate cross-functionally to support projects and continuous improvement.Lead contamination control e
An exciting opportunity has arisen for an Change Control Coordinator to join our client BD Medical in their MMS Operations team. The successful candidate will be responsible for the coordination and administration of change orders and supporting services, including facilitating cross-functional alignment and communication. Location: Winnersh, UK - hybrid role Pay rate: £17.95 per hourWorking hours: 09:00-16:30, 35 hours per week (30 min break unpaid daily)
An exciting opportunity has arisen for an Change Control Coordinator to join our client BD Medical in their MMS Operations team. The successful candidate will be responsible for the coordination and administration of change orders and supporting services, including facilitating cross-functional alignment and communication. Location: Winnersh, UK - hybrid role Pay rate: £17.95 per hourWorking hours: 09:00-16:30, 35 hours per week (30 min break unpaid daily)
Job Title: Lab Assistant - AccessioningPay rate: £25,500 PAWorkings hours: 8-4 Mon-FriLocation: LoughtonDuration: Sept end 2025 RESPONSIBILITIES: To undertake the day to day work programme in the laboratory to agreed deadlines and quality standardsensuring all samples delivered are handled according to current standard operating procedures.Receive goods delivered at the back door, transferring those containing samples to accessioning and notifying other de
Job Title: Lab Assistant - AccessioningPay rate: £25,500 PAWorkings hours: 8-4 Mon-FriLocation: LoughtonDuration: Sept end 2025 RESPONSIBILITIES: To undertake the day to day work programme in the laboratory to agreed deadlines and quality standardsensuring all samples delivered are handled according to current standard operating procedures.Receive goods delivered at the back door, transferring those containing samples to accessioning and notifying other de
ResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.Act
ResponsibilitiesLead and develop the local Regulatory Affairs team, setting clear goals, managing performance, and supporting training, mentoring, and resource planning.Prepare, review, and adapt CMC documentation using validated systems; monitor regulatory changes and assess impact across markets.Ensure alignment between registered dossiers and site operations; support GMP compliance, review regulated content, and assist during audits and inspections.Act
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
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
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
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
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
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.
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
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
Are you a skilled and motivated individual with an engineering background looking for a challenging and rewarding role with a leading medical technology company? A global leader in medical technology, is seeking a dynamic Moulding Production Technician to join a team in Plymouth. You'll be part of a cutting-edge manufacturing operation, playing a vital role in producing millions of life-saving medical devices each year. What You'll Do: Precision Manufactur
Are you a skilled and motivated individual with an engineering background looking for a challenging and rewarding role with a leading medical technology company? A global leader in medical technology, is seeking a dynamic Moulding Production Technician to join a team in Plymouth. You'll be part of a cutting-edge manufacturing operation, playing a vital role in producing millions of life-saving medical devices each year. What You'll Do: Precision Manufactur
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
