GMP Cleanroom Production Support Technician

Lonza Group Ltd.

Geleen

On-site

EUR 32,000 - 45,000

Full time

14 days+
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Benefits offered by this job

Competitive compensation
Career development
Structured manufacturing environment
Global benefits

Job summary

Lonza Geleen, Netherlands, is seeking a Production Support Associate to secure GMP manufacturing processes in a cleanroom environment. You will prepare, transport, and verify materials for production, and support daily manufacturing activities to ensure safety, quality, and efficiency.

This site-based role offers collaboration with Manufacturing, QA, QC, and Supply Chain, with a focus on detail, hands-on work, and clear pathways for growth in pharmaceutical and biotechnology manufacturing.

Qualifications

  • Hands-on approach and strong attention to detail.
  • Ability to follow established procedures and maintain high quality.
  • Strong communication skills and a collaborative mindset.
  • Ability to prioritize tasks and adapt in a dynamic manufacturing environment.
  • Motivation to learn new skills and develop in GMP manufacturing.

Responsibilities

  • Support daily manufacturing activities within a GMP cleanroom environment.
  • Prepare, transport, and verify materials required for production processes.
  • Perform cleanroom support activities, including cleaning and area preparation.
  • Conduct routine checks to ensure production areas and equipment are ready for manufacturing operations.
  • Follow GMP, safety, hygiene, and quality procedures accurately and consistently.
  • Work closely with Manufacturing teams and supporting departments to maintain efficient production schedules.
  • Identify, report, and support the resolution of process deviations or operational issues.

Skills

Hands-on
Attention to detail
Communication
Teamwork
Prioritization
Adaptability
Learning mindset

Education

MBO qualification
Technical/production education

Job description

Lonza Geleen, Netherlands, is seeking a Production Support Associate to secure GMP manufacturing processes in a cleanroom environment. You will prepare, transport, and verify materials for production, and support daily manufacturing activities to ensure safety, quality, and efficiency.

This site-based role offers collaboration with Manufacturing, QA, QC, and Supply Chain, with a focus on detail, hands-on work, and clear pathways for growth in pharmaceutical and biotechnology manufacturing.

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