- Overlooking manufacturing process improvements
- Reviewing validation activities and assuring appropriate risk management in the validation strategy
- Assessing change controls and building the technical strategy for implementation
- Supporting process technical transfer teams
- Supporting the introduction of new products
- Analysis of process data to support the launch
- Investigations of deviations and complaints
- Reviewing technical documentation and manufacturing instructions
- Ensuring that adequate documentation is available to support the successful registration of projects
- You will be working in cross-functional teams
- Min 5 years of experience in the pharmaceutical sector
- Experience with QA and validation activities
- Fluent in English
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QA / validation engineer - Brussels, België - EngiFlex
Beschrijving
Roles and responsabilities:
Profile:
What's in it for you
Full-time contract. (Freelance also possible)
You will be part of a growing Belgian SME where initiative and personal development are encouraged. We will provide you with an enjoyable work environment with fun colleagues. Well work out a career plan with you, with attention and a budget for extra education/certification. You can count on an attractive salary, supplemented with extra-legal benefits, including a company car.
