Regulatory Affairs Jobs in Devon
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Search results - Regulatory Affairs Jobs in Devon
Robert Walters Workforce Consultancy-Plymouth
Risk Consultant - Conduct & Culture
Business area: Risk and Compliance /Regulatory Affairs
Cardiff, Hove, Hybrid
Consultant
Purpose of role:
To support the Colleague Conduct and Culture Manager in the management and oversight of the L&G...
PQE Group-England
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? Management of qualification and test plans according to specific technical requirements, requirements-testing traceability...
Manucomm Recruitment-Exeter
Technical Assistant, QA Supervisor, Food Safety and Compliance Technologist, Regulatory Affairs Technologist, Product specifications Technologist or Compliance Technologist.
JBRP1_UKTJ...
EPM Scientific-England
EPM is partnered with a leading medical device company in the blood & cell therapy space seeking to add a Director of Market Access & Government Affairs to their Patient Access Leadership Team, which includes Medical Affairs, Government Affairs...
mindmatch.ai -
Robert Walters Workforce Consultancy-England
Risk Consultant - Conduct & Culture
Business area: Risk and Compliance /Regulatory Affairs
Hove/ Cardiff/ Hybrid
Consultant
Purpose of role:
To support the Colleague Conduct and Culture Manager in the management and oversight of the L&G...
Meet Life Sciences-England
registration and launch. Key Responsibilities: Provide medical and scientific expertise across clinical development projects Lead the clinical contribution to global drug development strategies Collaborate with cross-functional teams including Regulatory...
mindmatch.ai -
Membership Bespoke-England
Strong background in public policy, lobbying, and regulatory affairs
Skilled communicator with media experience and public speaking expertise
Adept at building industry alliances and influencing government policies
Strategic thinker with a vision...
Regulatory Affairs – Related jobs in Devon:
MCG Talent-England
media, and internal stakeholders. Government and Public Affairs: Serve as a liaison between the firm and government agencies, advising on public policy and managing communications around regulatory, legislative, and policy developments.
Provide senior...
mindmatch.ai -
SRG-England
in the local language while maintaining compliance with regulatory and company standards. You will also support second-line content management and escalation processes within a dynamic, multilingual medical information team.
Key Responsibilities
Customer...
Gilead Sciences, Inc.-England
Patient Safety, Regulatory Affairs, Clinical Operations, Medical Affairs and Global Value and Access, to anticipate and meet the evidence needs of regulators, payers, providers, and patients.
• Actively identify the need for the development of processes...
appcast.io -
Planet Pharma-England
best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC...
EPM Scientific-England
EPM is partnered with a leading medical device company in the blood & cell therapy space seeking to add a Director of Market Access & Government Affairs to their Patient Access Leadership Team, which includes Medical Affairs, Government Affairs...
RBW Consulting-England
Cross-Functional Collaboration Work closely with Pharmacy Managers and Medical Affairs teams to ensure aligned messaging and strategy. Collaborate with Marketing to develop territory-specific campaigns and engagement initiatives.
5. Compliance...
Norgine-England
of Expertise.
We have an exciting opportunity for a Associate Director Global Regulatory Affairs to join Norgine.
The person holding this position will report to the Director Global Regulatory Strategy Science and Evaluations and be a member...
workable.com -
Meet Life Sciences-England
Regulatory Affairs, Medical Affairs, Early Development, and Commercial teams
• Support the execution of CDPs and ensure scientific and operational excellence in clinical trials
• Participate in protocol development, trial design, and medical monitoring...
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