QA Systems Lead
As QA Systems Lead in Nivelles, you take process ownership of a core process in the pharmaceutical quality system, such as deviation, CAPA, change control or training. You join a pharmaceutical employer in Walloon Brabant on a permanent contract. You monitor KPIs and backlogs, help prepare inspections and coach users through digital or procedural improvements. A master's degree in a scientific field and solid GMP experience are your foundation.
What you'll do
- Take process ownership for deviation, CAPA, change control or training
- Monitor KPIs and backlogs within your quality process
- Monitor the quality of investigations and the related actions
- Facilitate governance and harmonisation of the quality system
- Help prepare your processes for inspections
- Coach users and implement digital or procedural improvements
What you bring
- You hold a master's degree in a scientific field
- You have solid experience in a GMP environment
- You have strong insight into quality systems and risk management
- You apply root cause analysis confidently in investigations
- You are an influential communicator who aligns multiple departments
What you get
- You get a key role in the pharmaceutical quality system
- You enjoy hybrid flexibility in your working week
- You collaborate in an international context
- You follow training to further develop your QA expertise
- You receive an attractive package at expert level
- You are hired 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.