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Regulatory Affairs Jobs in Berkshire

1 - 15 of 42
1 - 15 of 42
Search results - Regulatory Affairs Jobs in Berkshire
Transcrip Partners-Wokingham
support and for delivering regulatory documents and processes. Our team is growing, and we are searching for highly capable Senior Director to join us and support our clients.  •  Provide regulatory affairs expertise to clients seeking regulatory strategic...
mindmatch.ai -
Blackfield Associates-Reading
Our client, a pharmaceutical development company has a requirement for a Regulatory Affairs Director to join their UK team. This role is perfect for a senior manager/ experienced regulatory professional who is looking to head up Strategy...
Cpl Life Sciences-Windsor
Job Title: Regulatory Affairs Manager CTA, CTR (Consultant) Apply (by clicking the relevant button) after checking through all the related job information below. Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £50-55 per hour...
mindmatch.ai -
Blackfield Associates-Reading
Our client, a pharmaceutical development company has a requirement for a Regulatory Affairs Director to join their UK team. This role is perfect for a senior manager/ experienced regulatory professional who is looking to head up Strategy...
Cpl Life Sciences-Windsor
Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) If the following job requirements and experience match your skills, please ensure you apply promptly. Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £22-25 per...
mindmatch.ai -
Cpl Life Sciences-Windsor
Job Title: Regulatory Affairs Manager CTA, CTR (Consultant) Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £50-55 per hour (inside IR35) We are partnered with a leading Pharmaceutical organisation who are looking...
Reading
The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested...
cv-library.co.uk -
Cpl Life Sciences-Windsor
Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £22-25 per hour PAYE (inside IR35) We are partnered with a leading Pharmaceutical organisation who are looking...
Reckitt-Slough
in your area, ensuring tasks are completed effectively and efficiently. The experience were looking for  •  Proven track record in regulatory affairs, showcasing full proficiency in this roles requirements.  •  Proficient in multitasking, executing tasks...
mindmatch.ai -
SRG-Maidenhead
We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office...
Hays Specialist Recruitment-Reading
Your new company A global pharmaceutical/cosmetics business is looking to bring on a regulatory affairs consultant who specialises in UK&I markets with cosmetics products on a 6-month project. Your new role As the regulatory consultant for UK&I...
dwp.gov.uk -
Wokingham
may also have experience in the following: Clinical Scientist, Medical Device Researcher, Clinical Affairs Specialist, Regulatory Research Analyst, Biomedical Researcher, Scientific Data Analyst, Clinical Study Coordinator, Medical Research Associate...
cv-library.co.uk -
CK Group-Slough
to determine their suitability and effectiveness.  •  Create new SOPs for manufacturing processes and testing methods as needed.  •  Provides technical support to the European Regulatory Affairs team to ensure that Declarations of Conformity are prepared properly...
AWE-Reading
purposes.  •  Update and manage AWEs environmental sustainability dashboards.  •  Contribute to AWEs annual Environmental Sustainability & Governance report, including interface with corporate affairs.  •  Oversee the implementation of AWE's scope 3 strategy...
CK Group- Science, Clinical and Technical-Slough
and effectiveness. Create new SOPs for manufacturing processes and testing methods as needed. Provides technical support to the European Regulatory Affairs team to ensure that Declarations of Conformity are prepared properly. Support in generating Bill of Materials...
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