GMP Process and Operations Compliance Specialist
As GMP Process and Operations Compliance Specialist in Nivelles, you strengthen daily GMP compliance directly on the production floor. You work for a direct employer in biopharmaceutical operations in Walloon Brabant and turn deviations into sustainable improvements. You support deviation investigations, root cause analysis and CAPA, review changes and qualifications and coach teams during audits and inspections.
What you'll do
- Observe the processes on the production floor
- Advise teams on procedures, documentation and good practices
- Support deviation investigations, root cause analysis and CAPA
- Review changes, qualifications and operational readiness
- Follow up the compliance KPIs of the operations
- Coach the teams during audits and inspections
What you bring
- You hold a master's degree in life sciences, chemistry, engineering or pharmacy
- You have practical GMP experience in production, MSAT, QC or QA
- You like to be visibly present on the shop floor
- You approach compliance questions in an analytical and structured way
- You are strong in constructive coaching of operational teams
What you get
- You get a hands-on compliance role close to production
- You get training opportunities to develop further
- You work in an organisation with strong internal mobility
- You are offered a competitive salary package
- You join the employer directly on a permanent, full-time contract
Want to know more about this profession, the salary and the growth paths? Read the role profile: Quality engineer→
How your application works
- Introduction. We call you as soon as possible for a short introduction.
- Interview at the client. A good fit? We put you forward and plan the interview together.
- Offer and start. We guide you through to the signature, and beyond.