Manufacturing Process Engineer

Oxford Global Resources
is looking for a
Manufacturing Process Engineer
to support large‑scale biopharmaceutical production activities for a
10 months project
in Geel. The role focuses on ensuring stable, safe and compliant manufacturing operations, supporting process execution, troubleshooting, documentation, and continuous improvement within a cGMP environment.

Key Responsibilities

• Execute, monitor and analyse activities related to the manufacturing process.
• Ensure all process steps are performed safely and in full compliance with
  cGMP
  and internal procedures.
• Support production campaigns for
  Phase III clinical molecules
  , including: Buffer preparation, filtration steps, chromatography operations, TFF (Tangential Flow Filtration).
• Maintain accurate and traceable
  electronic and paper documentation
  .
• Ensure all activities meet regulatory, quality and safety standards.
• Identify opportunities to improve process efficiency, quality and safety.
• Contribute to the development and implementation of improvement initiatives.
• Evaluate process results, identify trends and propose corrective actions.

Requirements

• Bachelor's degree in Engineering, Biotechnology, Life Sciences or equivalent experience.
• 3–5 years
  of experience in biopharmaceutical manufacturing or process engineering.
• Strong understanding of
  cGMP
  , bioprocess equipment and production workflows.
• Hands‑on experience with buffer prep, filtration, chromatography and/or TFF.
• Ability to independently execute routine and non‑routine manufacturing activities.
• Strong analytical mindset and ability to interpret process data.
• English required; Dutch is an advantage.