Available Jobs
Senior / Principal Regulatory Writer |
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Location: UK Recruiter: Barrington James Job Hours: Full-time |
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SENIOR MEDICAL WRITER (Germany, UK, USA, Canada, Portugal, Italy, Ireland) Only candidates who meet the following requirements will be considered: Candidate must live in one of the following countries: Germany, UK, USA, Canada, Portugal, Italy, Ireland. Applicants will work from one of our offic... | ||||
Senior Manager Regulatory Affairs |
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Location: Cambridge Recruiter: Quanta Part Of QCS Staffing Job Hours: Full-time |
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Senior Manager Regulatory Affairs - Pharmaceuticals - Cambridge Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Senior Manager Regulatory Affairs. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its exp... | ||||
Regulatory Advisor |
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Location: Cambridge Recruiter: Arcadis Job Hours: Full-time |
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Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 36, people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curiou... Read More | ||||
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... | ||||
Quality Assurance And Regulatory Affairs Specialist |
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Location: Cambridge Recruiter: Origin Sciences Job Hours: Full-time |
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Origin Sciences is a start-up biotechnology company based in Granta Park, just south of Cambridge. We develop our own innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank provides clinical material for our research and development... Read More | ||||
Regulatory Affairs Manager |
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Location: Cambridge Recruiter: Proclinical Job Hours: Full-time |
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Proclinical is seeking a Regulatory Affairs Manager. This role is pivotal in providing country-specific regulatory expertise and execution for the management of biotechnology products. The successful candidate will be responsible for coordinating and carrying out regulatory submissions in compliance... Read More | ||||
Associate Director, Regulatory Affairs CMC |
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Location: Cambridge Recruiter: Gilead Sciences International Job Hours: Full-time |
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Description We are looking for an experienced Regulatory professional to join our global team. Location: Cambridge or Uxbridge. In this role, you will be responsible for acting as one of the EU Regulatory leads for Kite's existing commercial and/or clinical programs. Your duties w... | ||||
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 ... | ||||
Associate Director, Regulatory Affairs CMC |
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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 | ||||
Global Regulatory Affairs Lead |
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Location: Cambridge Recruiter: Sanofi Job Hours: Full-time |
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Job title: Global Regulatory Affairs Lead Location: Cambridge, MA or Bridgewater, NJ About the job The Global Regulatory Affairs Lead (GRL) is the fully accountable decision maker for the development & execution of creative, thoughtful, and robust global regulatory strategies for their pr... Read More |