Clinical Supply QP Partner
As Clinical Supply QP Partner in Waterloo, you carry quality responsibility for the release and compliance of clinical medicines. You work for a direct employer in clinical medicines supply in Walloon Brabant and assess batch records under GMP. You advise on production, packaging, import, storage and distribution and handle deviations, recalls and quality risks, so that clinical products are available on time.
What you'll do
- Assess the batch records of clinical products
- Certify release decisions as QP or support them
- Advise on the production, packaging and import of clinical medicines
- Advise on the storage and distribution of clinical products
- Handle deviations, recalls, changes and quality risks
- Work with clinical operations, manufacturing and external partners on timely supply
What you bring
- You are a registered pharmacist with a valid registration
- You are eligible as Qualified Person under the applicable regulations
- You have extensive GMP experience with clinical or commercial medicines
- You form an independent quality judgement on releases
- You have strong skills in working with stakeholders
- You work in professional English within an international context
What you get
- You get a responsible role as Qualified Person
- Your role has a clear international reach
- You can work hybrid, partly from Waterloo
- You receive a competitive package at senior level
- 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.