Join a global healthcare leader as a Process Operator, where you'll ensure efficient, high-quality manufacturing in a GMP-regulated setting. Collaborate with a self-directed team to manage assembly, processing, machinery operation, and packaging. Your role is crucial in delivering pharmaceutical products on time, while driving continuous improvement. Enjoy unique perks such as professional development opportunities and a supportive work environment that values innovation and excellence. Keep reading to see why we could be the perfect match for you.

Over het bedrijf

SIRE Life Sciences

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The Company
Our client is a global healthcare company focused on discovering, developing, and providing innovative medicines, vaccines, and animal health products. With a strong emphasis on research and development, it is committed to improving patient outcomes and addressing unmet medical needs across various therapeutic areas, including oncology, immunology, cardiology, and infectious diseases.

About the Role
As a Process Operator, you’ll play a vital role in ensuring smooth, efficient, and high-quality manufacturing processes within a GMP-regulated environment. You will be part of a self-directed production team, executing day-to-day operations such as assembly, processing, machinery operation, and packaging. Your work will support the timely and compliant delivery of pharmaceutical products, while also contributing to continuous improvement and operational excellence.

Responsibilities
- Execute production activities according to daily schedules, ensuring adherence to GMP standards and safety (EHS) regulations
- Operate machinery and equipment for pharmaceutical manufacturing, including set-up, monitoring, and shut-down procedures
- Perform all necessary preparatory and finishing tasks to ensure production readiness and cleanliness in qualified areas
- Monitor and document production processes to support batch documentation and data integrity
- Coordinate with planning and supply chain teams to align materials, resources, and equipment for optimal workflow
- Contribute to routine maintenance and troubleshooting of production equipment

Requirements
- MBO degree in a technical, production, or life sciences field with 1–3 years of relevant experience
- Experience in pharmaceutical or GMP-regulated manufacturing is preferred
- Familiarity with production documentation and batch records is a plus
Strong awareness of EHS and GMP guidelines
- Good communication skills in both Dutch and English

Other Information
The position is designed to be a long-term, permanent role.

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