Available Jobs
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Senior Regulatory Affairs Specialist |
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Location: Cirencester Recruiter: Corin Group Job Hours: Full-time |
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| Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to support pre- ... Read More | ||||
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Senior Regulatory Affairs Specialist |
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Location: Cirencester Recruiter: Corin Group Job Hours: Full-time |
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| Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to support pre- ... Read More | ||||
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Regulatory Affairs Manager |
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Location: Cambridge Salary: £50,000 per year Recruiter: Cpl Life Sciences Job Hours: Full-time |
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| Overview Job Title: Regulatory Affairs Manager (Food & Beverages) Job Type: Permanent position Location: Chiswick, Cambridge, or Manchester – 2 days on-site per week. Remuneration: £50,000 – £55,000 + benefits This is an excellent opportunity to join a family-owne... | ||||
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Associate Director - Regulatory Affairs |
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Location: Cambridge Recruiter: Gilead Sciences International Job Hours: Full-time |
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| Description Regulatory Affairs Associate Director Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987, that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. Toget... | ||||
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Regulatory Affairs Manager |
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Location: Witney Recruiter: Abbott Job Hours: Full-time |
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| Abbott Diabetes Care designs, develops and manufactures leading-edge glucose monitoring systems and test strips for use in both home and hospital settings. Our product portfolio includes Freestyle Libre, a recently launched system that is revolutionising how people with diabetes around the world mon... Read More | ||||
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Senior Regulatory Affairs Specialist |
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Location: Cirencester Recruiter: Corin Job Hours: Full-time |
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| Senior Regulatory Affairs Specialist Corinium Centre, Love Lane Industrial Estate, Cirencester GL7 1YJ, UK Req #233 04 April 2024 Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all regulatory aspects of post-market surveillance. The Reg... Read More | ||||
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Regulatory Compliance Engineer |
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Location: Charfield Salary: £55.00 per hour Recruiter: Renishaw Job Hours: Full-time |
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| Job Description Medical Devices, EMC, Safety Salary approx. £55-£60k (dependent on experience) Hybrid working 2 days/week site based with additional days depending on business needs. We are looking for an experienced regulatory compliance engineer to join our team and help us ensure that our ... Read More | ||||
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Associate Director - Regulatory Affairs |
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Location: Cambridge Recruiter: Gilead Sciences Job Hours: Full-time |
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| Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across ... Read More | ||||
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Associate Director, Regulatory Affairs |
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Location: Cambridge Recruiter: Relay Therapeutics Job Hours: Full-time |
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| The Opportunity: We are looking for a strategic regulatory leader to join our growing regulatory team at Relay Tx. You will have the opportunity to define and implement innovative regulatory strategies to expedite the development and approval of our transformative pipeline. You will serve as ... | ||||
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Regulatory Affairs Manager - CMC |
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Location: Cambridge Recruiter: Parkside Job Hours: Full-time |
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| My client is a global biopharma company. They are seeking a Regulatory Affairs Manager (CMC) to join our Regulatory Affairs Team based in Cambridge on a 12 month contract. Hybrid working Key Responsibilities Co-ordinate the preparation of high quality CMC documents to support regulatory subm... | ||||
