Contract Regulatory Specialist Jobs
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Regulatory Affairs Consultant
We are looking for an experienced Regulatory Affairs Consultant to support MDR transition, risk management, and validation documentation activities within a highly regulated pharmaceutical/medical device environment. This 12‑month hybrid assignment is based in Antwerp, working 2-3 days on‑site. Key ResponsibilitiesUpdate and rewrite Risk Management...
Regulatory Affairs/ CMC Consultant
We are seeking an experienced Regulatory & CMC Lead to guide the chemistry, manufacturing, and controls strategy for a regulated cannabis inhalation product targeting medical and medically‑adjacent markets. This is a part‑time, long‑term contract role focused on building pharma‑grade documentation, specifications, and regulatory readiness appropria...
Regulatory Specialist
Regulatory Specialist (Contract - W2 Only)Location: Remote (occasional travel within the U.S.) Contract Length: 2 Years Hours: 40 per week Start Date: ASAPAbout the RoleA leading global MedTech client is seeking an experienced Regulatory Specialist to support regulatory strategy and submissions for their orthopaedic device portfolio. This is an exc...
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Regulatory Affairs Consultant (Freelance)
Regulatory Affairs Consultant (Freelance) Location: Brussels, Belgium (hybrid)Length: 12 months (possibility of extension)Start Date: June 2026 Key ResponsibilitiesSupport the development and maintenance of regulatory strategies for new and existing medical device products, including involvement with a Class IIb device.Contribute to regulatory proj...
Freelance Consultant Software as a Medical Device (SaMD)
We're looking for an experienced freelance consultant to support regulatory and quality activities across a range of complex medical devices. This role suits someone who has worked with life‑sustaining, electromechanical, infusion, monitoring, renal, or surgical technologies and understands the demands of global compliance.What You'll DoDevelop reg...
Regulatory Specialist
Regulatory Affairs Specialist (12‑Month Contract)Focus: 510(k) FDA Submission - Cardiology Medical DevicesOverviewWe are seeking an experienced Regulatory Affairs Specialist to support the preparation, execution, and submission of a 510(k) premarket notification for an innovative cardiology medical device. This is a 12‑month contract role with resp...