Regulatory Affairs Jobs in Merseyside
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Search results - Regulatory Affairs Jobs in Merseyside
Scendea-England
knowledge in product development and international regulatory affairs.
• Create and deliver high-quality billable regulatory related documentation for clients, contributing to the technical authorship and review of development regulatory documents including...
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...
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 -
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...
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 -
Planet Pharma-England
recognized by FORBES as the 17th 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...
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 -
Regulatory Affairs – Related jobs in Merseyside:
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...
KBC Technologies Group-England
and Manchester with flexibility to travel to site locations Cambridge or Macclesfield as required) Hybrid: 3 days a week working from office 6 months extendable contract Job Description: Lead business consulting engagements within Medical Affairs, Regulatory...
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...
Konecta-England
Market Region (UK, USA, South Africa) , focusing on commercial law, M&A, and corporate matters. This individual will play a key role in managing the company’s legal affairs in a fast-paced and dynamic environment within the BPO, AI, and tech industries...
mindmatch.ai -
Planet Pharma-England
to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities...
BDO UK-England
in the right place.
Tax is a dynamic, ever-changing industry. As our clients’ needs and the regulatory environment evolve, you’ll encounter new problems to solve and new opportunities for growth. You'll be advising clients on their high-profile M&A activity...
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...
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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