Contract Jobs in Belgium
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Process Safety Specialist (HAZOP/LOPA Facilitation Lead)
Location: Geel, Belgium (with occasional travel to another local site) Contract Duration: ASAP - 31 December 2026 (extension possible) Work Authorization: No sponsorship available - candidates must have valid EU right to work Overview We are seeking an experienced HAZOP/LOPA Lead to join a leading pharmaceutical manufacturing site in Belgium. You w...
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...
Post Market Surveillance Analyst
Job Title: Post Market Surveillance Specialist (Contract)Location: Brussels, Belgium (3 days onsite / 2 days remote)Duration: 8-month contractHours: 40 hours per weekStart Date: AugustLanguage: English (strong communication required)Industry: Medical Device / Pharmaceutical About the Role A leading medical device company is seeking a Post Market Su...
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Regulatory Affairs Consultant (SaMD)
Location: Brussels, Belgium (1-2 days per week on site)Start Date: Ideally ASAPContact: 12 months (freelance engagement) About the RoleWe're looking for an experienced consultant to advise on regulatory and quality strategies for software-driven medical technologies. This role is ideal for someone who understands the complexities of compliance for ...
Quality Specialist
Quality Specialist (Freelance - 12 Month Contract) Brussels, Belgium | Hybrid (3 days onsite / 2 days remote)Contract | Medical Device | No Sponsorship Available We are currently seeking an experienced Quality Specialist to join a leading medical device organisation based in Brussels on a 12-month freelance contract. This role offers the opportunit...
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...