QC Specification Specialist
As QC Specification Specialist in Nivelles, you manage the analytical specifications on which biopharmaceutical quality control relies. You work for a direct employer in biopharmaceutical QC in Walloon Brabant and make sure test requirements remain scientifically correct and GMP-compliant. You create and modify specifications, analysis codes and master data and assess the impact of method and process changes together with QC, QA and regulatory.
What you'll do
- Create and modify specifications and analysis codes
- Manage the associated master data in the systems
- Align requirements with QC, QA, regulatory and product experts
- Assess the impact of method and process changes on specifications
- Support deviations and audits related to specifications
- Contribute to improvements in data quality and document management
What you bring
- You hold a master's degree in chemistry, pharmacy, biochemistry or a comparable field
- You have experience with QC and GMP documentation
- You know analytical test methods from practice
- You work accurately and look critically at requirements
- You collaborate smoothly in English with colleagues
What you get
- You get a substantive quality role in biopharmaceutical QC
- You have the option to work hybrid
- You get opportunities to develop further scientifically
- You receive a strong benefits package from the pharmaceutical sector
- 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.