Clinical Packaging & Labelling Operator

Company
Our client is a global, innovation-driven life sciences organization that supports clinical trials worldwide. The Breda site plays a critical role in ensuring investigational medicines are labelled, packaged, and prepared accurately and safely for patients, working to strict quality standards in a regulated environment.

Job Description
For our client in Breda, we are looking for a Clinical Packaging & Labelling Operator (GMP) to join a dedicated team responsible for manual labelling, packaging, and assembly activities for clinical trial materials. The role is hands-on and detail-focused, with work carried out mainly at room temperature and occasionally in cold-room conditions (2-8°C). Accuracy, teamwork, and flexibility are essential.

Responsibilities
- Execute manual clinical labelling and packaging activities according to SOPs and quality guidelines
- Work with trial-specific configurations, ensuring every packaging step is performed correctly and documented properly
- Support packaging operations in both room temperature and cold-room environments when required
- Take ownership of daily tasks and results within their working area, focusing on right-first-time execution
- Escalate issues when necessary and contribute to smooth, compliant operations
- Complete all assigned trainings in line with the training plan and required timelines
- Carry out batch-related logistics activities linked to packaging operations
- Actively look for improvements and efficiency opportunities in processes and ways of working

Requirements
- Experience in a manual packaging environment (preferably within pharma or another GMP/GDP-regulated setting)
- Comfortable working in a strongly regulated quality environment with a high level of documentation and precision
- Quality- and performance-driven, with a proactive and learning-oriented mindset
- Strong team player with clear communication skills
- Able to work accurately, efficiently, and stay effective when priorities change
- Experience with SAP and/or MES is an advantage

Other Information
This is an on-site role based in Breda, Netherlands, working in a collaborative day-shift team environment where careful handling and attention to detail directly supports clinical trial patients.
If you are interested and want to apply, please submit your application via the apply button below and contact me.

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