We are a Belgian engineering consulting firm that assists SMEs and large industrial organizations in bringing their innovation and R&D initiatives to life.
Job Description
- Responsible for the validation according to the current GMP guidelines for an automated control system:
- Writing commissioning and qualification tests based on user requirements and functional specifications
- Executing tests in an accurate and GMP manner
- Performing risk assessments
- Point of contact for validation topics, both internal and external
- Work in a project team, follow up on schedules and milestones
Required qualifications
- Experience with GAMP5, 21CFR part 11 and computer system validation
- Affinity with computerized systems, such as PLC, SCADA,…
- Fluent in Dutch and English
- Good analytical & communication skills
- Willingness to travel (sporadically)
- Bachelor or higher technical degree
- At least 2 years relevant (pharmaceutical GMP environment) experience
- Knowledge of office applications: Word, Excel, Outlook
Benefits
We offer you a position as a consultant within the fascinating world of high tech and innovation. We provide a complete package with on one side training, coaching and a close follow-up, and on the other side a balanced salary package with fringe benefits based on your capabilities and experience.
Working with us means choosing a long-term perspective, development possibilities, and a personal approach. A human-centered, diverse company that values and supports your physical and mental well-being.
