Regulatory Specialist jobs

• Paris
• Negotiable
• Posted 12 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 13 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 14 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 24 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 24 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...

• 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...