Computerized System Validation (CSV) Engineer | Life Science - Brussels - French speaking

One of our Blue Chip Clients is urgently looking for a Computerized System Validation (CSV) Engineer | Life Science.

Please find some details below:

Job Description

• As a Computerized System Validation Engineer, you will play a crucial role in ensuring that all computerized
• systems related to Good Manufacturing Practices (GMP) are validated and function as intended.
• Depending on your project, your role will involve:
• Writing and reviewing validation plans (VP) and validation summary reports (VSR).
• Reviewing and approving design documentation to ensure alignment with system requirements and GMP
• guidelines.
• Writing and reviewing qualification protocols and reports (IQ/OQ & PQ).
• Monitoring the execution of qualification and validation activities.

Your Profile

• As an engineer, you possess the following skills:
• Master's degree in engineering (or equivalent experience).
• Experience with GMP and specific regulations and guidelines applicable to computerized and automated
• systems (GAMP, Eudralex Vol 4 Annex 11, 21 CFR Part 11, etc.).
• Experience with validation practices and guidelines (V-cycle, ICH, ASTM E2500, etc.).
• Proficiency in English and French.
• Relevant experience in the pharmaceutical industry is a plus.

Please send CV for full details and immediate interviews. We are a preferred supplier to the client.