Regulatory jobs

• Copenhagen
• Negotiable
• Posted 7 days ago

We are working with a leading pharmaceutical company based in Copenhagen that are dedicated to the development, manufacturing, and commercialisation of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-o...

• Negotiable
• Posted 8 days ago

EPM is urgently looking for a freelance Regulatory/Clinical Affairs Specialist to support one of our key medical device clients on a 12-month assignment as soon as possible. Below is a brief overview of the role and its requirements: Regulatory Affairs / Clinical Affairs Specialist Medical Device...

• Paris
• Negotiable
• Posted 10 days ago

My client is building the first universal AI Operating System to lay the foundation for Biological Artificial Superintelligence (BASI). This OS integrates a suite of AI agents that decode complex biology, accelerate research, and dramatically increase productivity. Acting as copilots,My clients a...

• Paris
• Negotiable
• Posted 10 days ago

Job Title: Senior Regulatory Affairs Specialist Location: France (Hybrid) Start Date: Within the next month Job Type: Full-time (Consultant, Freelancer, or Contractor) Industry: Medical Devices Key Responsibilities: Documentation Specialist: Lead and manage all regulatory documentation processes,...

• Massachusetts
• Negotiable
• Posted 12 days ago

We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulati...

• Northern Ireland
• Negotiable
• Posted 22 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clinical trials. GAP Asse...

• Northern Ireland
• Negotiable
• Posted 22 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clini...

• Northern Ireland
• Negotiable
• Posted 29 days ago

We have a current opportunity for a Senior Clinical Project Manager working with IVDs on a contract basis. 6 months contract (possible extension) Clinical protocols, risk management plans, knowledge of IVD regulation within Europe Client-facing position (face-to-face) Remote with occasional site ...

• Morristown
• Negotiable
• Posted about 1 month ago

Job Title: Senior Associate, Regulatory Affairs Location: Morristown, New Jersey About the Role: We are seeking a highly motivated and detail-oriented Senior Associate, Regulatory Affairs to join our team. In this role, you will help author, compile, review, and submit high-quality regulatory sub...

• United States of America
• Negotiable
• Posted about 1 month ago

* Authoring high-quality CMC documentation for US/ EU / UK countries, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. * P...

• Nottingham
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.

• United States of America
• Negotiable
• Posted about 1 month ago

A leading organization in the pharmaceutical and regulatory affairs industry, dedicated to increasing project efficiency and establishing project management standards; are looking for a talented and experienced Project Manager to join the Project Management Office (PMO) team. Key Responsibilities...

• Barcelona
• Negotiable
• Posted about 2 months ago

I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team. Ideal Profile: Experience in regulatory strategies and documentat...