cGMP Engineer

Turn deviations into solutions in a fast-paced cGMP biotech environment.

R&D Partners is seeking a skilled cGMP Engineer to join a leading biotechnology company in Belgium. This is a fully onsite, project-based role requiring contractors with 2-5 years of practical experience to support deviation handling during campaigns.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Manage and resolve deviations.
• Provide support during inspections.
• Execute CAPA (Corrective and Preventive Actions), CCR (Change Control Requests), and document changes.

Key Skills and Requirements:

• Strong knowledge of cGMP (current Good Manufacturing Practices).
• Solid understanding of manufacturing processes.
• 2-5 years of hands-on experience in a similar role.

For more information, please contact Grant Van Schalkwyk.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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