Available Jobs
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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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Quality Assurance Regulatory Affairs Manager |
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Location: Usk Recruiter: Independence Products |
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| Are you up for the challenge of bringing disruptive new technologies to the market for patients with chronic medical conditions? We are rapidly expanding and are looking for an experienced Quality & Regulatory Affairs Manager with experience of managing Class I, II, medical devices. About Job: As ... | ||||
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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 / 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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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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Regulatory Specialist I |
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Location: Milton Keynes Recruiter: Sensient Technologies Job Hours: Full-time |
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| At Sensient Technologies , we are experts in the science, art and innovation of color and flavor. We are market savvy and visionary. We are problem solvers. And we will be better with you. We are looking for a Regulatory Specialist to join the Flavors business in Europe . This position is a key me... Read More | ||||
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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... | ||||
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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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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... | ||||
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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 | ||||