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.