Available Jobs
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Senior Regulatory Affairs Manager CMC |
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Location: Cambridge Recruiter: Pharma Partners Recruitment Job Hours: Full-time |
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| Job title: Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities. Candidates mus... | ||||
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Regional Regulatory Affairs Lead |
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Location: Buckinghamshire Salary: £45,000 per year Recruiter: Harrison Scott Associates Job Hours: Full-time |
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| Job Title: Regional Regulatory Affairs Lead Salary: £45-55k basic + benefits Location: Buckinghamshire Reference: J78872 Contact: Telephone: 0141 647 6688 Categories: , , The Company We are working with a group that owns a some of the most iconic sweet and savoury food bra... | ||||
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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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Senior Regulatory Affairs Specialist |
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Location: Cardiff Salary: £40,000 per year Recruiter: Yolk Recruitment Job Hours: Full-time |
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| Senior Regulatory Specialist Cardiff £40,000 - £50,000 Yolk Recruitment is partnered with a pioneering medical device business during an exciting period of sustained expansion and has a new opportunity for a Regulatory Specialist to join the team. The role offers not only the opportunity to ... Read More | ||||
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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... | ||||
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Regulatory Affairs Specialist |
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Location: Oxford Recruiter: Oxford Nanopore Technologies Job Hours: Full-time |
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| About Us Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and commercial presence in many global locations across the US, APAC and Europe. Oxford Nanopore employs from multiple subject areas including nanopore science, molecular bi... Read More | ||||
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Senior / Principal Regulatory Writer |
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Location: United Kingdom 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... | ||||
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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 | ||||
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Regulatory Affairs Associate |
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Location: Caerphilly Salary: £45,000 per year Recruiter: Hunter Selection Job Hours: Full-time |
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| £45000 - £48000 per annumCaerphilly Regulatory Affairs Associate Regulatory Affairs Associate Caerphilly CF83 Commutable from Blackwood, Caerphilly, Newport, Heads of the Valleys, Merthyr Tydfil, Aberdare, Abertillery, Cardiff, Pontypridd £45,000 Benefits 25 d... | ||||
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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 ... | ||||
