QC Specification Specialist
Ready to start as a QC Specification Specialist in Nivelles? Our client in biopharmaceutical quality control hires you directly. In this role you manage analytical specifications and make sure test requirements remain scientifically correct and GMP-compliant. You get a clear set of responsibilities, short lines to colleagues and partners, and room for your own initiative.
What you'll do
- Create and modify specifications, analysis codes and associated master data
- Align requirements with QC, QA, regulatory and product experts
- Assess the impact of method and process changes on specifications
- Support deviations, audits and improvements around data quality and document management
What you bring
- Master's degree in chemistry, pharmacy, biochemistry or comparable
- Experience with QC, GMP documentation and analytical test methods
- Accurate, critical and fluent in collaboration in English
What you get
- A substantive quality role with hybrid options, scientific development and a strong pharmaceutical benefits package
- Hybrid working arrangement
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.