9 Contract Pharmaceutical found

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

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 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.

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

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