Join a global healthcare leader known for its commitment to innovation, quality, and patient safety. Our site in Geel is part of a wider network that delivers life-changing medicines to patients around the world. You'll be part of a team that values collaboration, continuous improvement, and professional development.
We are looking for a Cleaning Validation Engineer to support cleaning compliance and validation activities within pharmaceutical and API manufacturing environments
Key Responsibilities:
* Support cleaning validation activities for pharmaceutical and API manufacturing.
* Prepare and maintain validation documentation (protocols, reports, SOPs).
* Execute cleaning validation studies and ensure regulatory compliance.
* Assist in investigations and contribute to CAPAs.
* Collaborate with teams on product introductions and process changes.
* Conduct periodic reviews and support audit readiness.
Role Requirements:
* Recent experience (within the last 3 years) in cleaning validation within a GMP-regulated pharmaceutical or API environment.
* Professional proficiency in Dutch (spoken and written).
* Availability to work 3–4 days on site in Geel.
* Suitable for junior-level candidates – no requirement to lead teams or drive change management, but must be capable of independently progressing tasks.
* Strong documentation and communication skills.
* Familiarity with automated control systems (e.g., DeltaV, SCADA) is a plus.
If Interested please apply!