Contract Regulatory Specialist Jobs
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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 Affairs Submissions Consultant
Regulatory Affairs Consultant Opportunity - EU/UK Submissions Specialist 📢 We are currently looking for an experienced Regulatory Affairs consultant / freelancer to support ad hoc regulatory submission activities on a fully remote basis. This is an excellent opportunity for a hands-on RA professional with strong operational submission experience a...
Regulatory Affairs Consultant (Freelance)
Regulatory Affairs Consultant (Freelance) Location: Wavre, Belgium (Hybrid) Contract: 12 months (extendable) Start: July 2026 Key ResponsibilitiesDefine and implement US regulatory strategy to support FDA approval of a Class III device undergoing clinical investigation.Author, review, and maintain technical and regulatory documentation, including I...
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Occupational Health Specialist
Occupational Health and Safety Specialist Overview:🏢 OverviewWe are supporting a leading, highly regulated organisation in the search for an Occupational Health & Safety Specialist on a 12-month contract basis.This role will have a strong Occupational Health and Industrial Hygiene focus, supporting the development and delivery of health-led safety...
QA/RA Specialist: Dental/Additive Manufacturing (Freelance)
QA/RA Specialist: Dental/Additive Manufacturing Location: Eindhoven, Netherlands (Hybrid / Remote)Engagement: Part-time contract | Start ASAP | 6-12 months An innovative medical device company in Eindhoven is seeking an experienced Medior to Senior QA/RA professional to support regulatory and quality activities for dental and/or additive manufactu...
Regulatory Affairs Consultant (Freelance Medical Devices)
Regulatory Affairs Consultant (Freelance - Medical Devices)Location: Grenoble, France (hybrid - on‑site presence with flexibility) Contract Length: 12 months (strong likelihood of extension) Start Date: May 2026Key Responsibilities:Contribute to the definition and execution of EU MDR regulatory strategy for both new development and lifecycle produc...