Biopharmaceutical Production Technician, Boxmeer, Noord-Brabant

The Company
A well-established company within the pharmaceutical and animal health industry, operating multiple production facilities across the Netherlands. The organization is recognized for maintaining high standards in GMP compliance, operational excellence, and innovative manufacturing technologies.

About the Role
As a Biopharmaceutical Production Technician, you will support bacteriological manufacturing activities by preparing, sterilizing, and supplying materials and equipment required for antigen production. Working in a regulated production environment, you will collaborate closely with operators and support teams to ensure efficient production flow, strict adherence to GMP standards, and accurate documentation. The role provides hands-on exposure to modern cultivation and single-use bioprocessing technologies.

Responsibilities
- Coordinate the flow of materials, including receipt, storage, and internal distribution.
- Operate and monitor sterilization equipment such as autoclaves.
- Prepare growth media and support cleaning and sterilization of mobile vessels and equipment.
- Ensure production teams have timely access to required materials and tools.
- Support manufacturing processes using advanced cultivation systems, from pilot scale to large single-use bioreactors (up to 1500L).
- Complete and maintain GMP records in line with regulatory requirements.
Report and follow up on deviations, equipment issues, and process observations.
- Actively contribute to continuous improvement initiatives within a Lean/Six Sigma framework.
- Collaborate with operators, media preparation teams, and production coordinators.

Requirements
- Completed MBO level 3 education or higher.
- Interest or experience in pharmaceutical or biotechnology manufacturing.
- Strong focus on quality, safety, and compliance.
- Good communication skills in Dutch, both spoken and written.
- Experience working in cleanroom environments is an advantage.
- Familiarity with SOPs, deviations, and equipment documentation.
- Prior experience in a GMP-regulated environment is a plus.

Other Information
- Day shift position with working hours from 07:00 to 15:30.
- Training and development opportunities, including Lean and Six Sigma programs.
- Opportunity to grow within a dynamic and expanding production organization.

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