Job Opportunity: CSV Specialist (12-month contract, Belgium)
We are looking for a French-speaking CSV (Computer Systems Validation) specialist to join a leading Belgium-based pharmaceutical company for a 12-month contract (3 days on-site per week).
Key Requirements:
* 4-8 years’ experience in CSV in a regulated environment
* Fluent French (verbal & written)
* Max 4 weeks’ notice period
* Hands-on experience in biologics or sterile commercial manufacturing
* Familiarity with GAMP-5 methodology
* Exposure to large pharma manufacturing environments is a strong plus
Responsibilities:
* Execute CSV activities across computerized systems in a GMP environment
* Create/execute validation plans, protocols (IQ/OQ/PQ), reports and lifecycle documentation
* Ensure compliance with regulatory standards and GxP within a biologics/sterile manufacturing setting
* Collaborate with cross-functional teams (IT, QA, manufacturing) on system qualification and compliance
Contract Details:
* Duration: 12 months
* Location: Belgium site (3 days/week on-site)
* Start: late 2025/early 2026
If you have the required experience and are ready to bring your CSV expertise into a dynamic manufacturing environment, please get in touch with your CV and availability
dominic.pritchard@biotalent.ch / +41415625046