Clinical Packaging & Labelling Operator

Sire Search; Breda; On-site; EUR 32,000 - 42,000; Full time

Job summary

Sire Search is seeking a Clinical Packaging & Labelling Operator (GMP) for our Breda site. The role involves hands-on manual labelling, packaging and assembly for clinical trial materials, mainly at room temperature with occasional 2–8°C conditions.

You will work in a regulated, quality-focused environment with strong emphasis on accuracy and documentation. As part of a dedicated team, you will ensure batch integrity, participate in training plans and contribute to compliant packaging

Qualifications

• Experience in a manual packaging environment (pharma or GMP/GDP-regulated setting).
• Experience with SAP and/or MES is an advantage.

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.

Skills

Manual packaging

SAP/MES experience

Tools

SAP

MES

Job description

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.