Contract Regulatory Specialist Jobs
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Principal Reg Specialist
Influence Regulatory Strategy for Products That Reach Global MarketsThe OpportunityA global medical device manufacturer is looking for a Regulatory Affairs Specialist to join a well-established regulatory team supporting a diverse product portfolio.This is a role for someone who wants to move beyond transactional regulatory work and become a valued...
Sr. Regulatory Affairs Consultant
Contract: 12-month, full time contractStart date: ASAP Client: US based large MedTech Working hours: Supporting US Team, some requirements for availability in CST time zoneJob Description:Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategiesParticipates in advocacy activities of a more ad...
Regulatory Affairs Specialist
Regulatory Affairs Specialist (Freelance) Location: Lyon, France (hybrid)Length: 12 months (possibility of extension)Hours: Full-time (40 hours per week)Start Date: Mid-August - September 2026Engagement: Freelance Key ResponsibilitiesContribute to the development and maintenance of regulatory strategies for both existing and new medical device pro...
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Regulatory Affairs Specialist
Job Title: Regulatory Affairs SpecialistDuration: 12 months (with extension opportunity)Hours: Full-time (hybrid/remote)Location: Paris, France Core ResponsibilitiesDesign and implement verification and validation protocols that meet international regulatory standards.Lead the selection and approval of testing partners under global certification sc...
Regulatory Affairs Consultant (Freelance)
Regulatory Affairs Consultant (Freelance) - Medical Devices Location: Brussels, Belgium (hybrid)Length: 12 months (possibility of extension)Start Date: ASAP We are partnered with a growing medical device manufacturer seeking an experienced Regulatory Affairs Consultant (Freelance) for a 12‑month engagement. This is an urgent requirement, and the co...
Sr. Regulatory Affairs Consultant
Contract: 12-month, full time contractStart date: ASAP Client: US based large MedTech Working hours: Supporting US Team, some requirements for availability in CST time zoneJob Description:Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategiesParticipates in advocacy activities of a more ad...