Technical Operator – Semi-Automated Lines

Technical Operator voor semi-automatische productielijnen bij een farmaceutische fabrikant in Breda, fulltime, GMP-omgeving.

Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)

Eisen

  • Proactive, accurate, and quality-focused
  • Experience with SAP and/or MES systems
  • Experience operating production, assembly, labeling, or packaging equipment
  • Experience working within GMP or another regulated manufacturing environment
  • Willing to work in 3-shift and future 5-shift rotations
  • Technical understanding of manufacturing processes and equipment
  • Fluent in English
  • MBO degree or equivalent technical background
  • Strong analytical and troubleshooting skills

Wensen

  • Experience with Root Cause Analysis (RCA), 5 Why, or similar methodologies
  • Knowledge of Lean or Continuous Improvement methodologies
Volledige omschrijving

Join a leading international pharmaceutical manufacturer where medicines are labeled, assembled, stored, and distributed worldwide. Working in a GMP-regulated production environment, you will help ensure reliable manufacturing processes while contributing to product quality and continuous improvement. As a Technical Operator – Semi-Automated Lines, you will operate and monitor semi-automated production equipment to ensure safe, efficient, and compliant manufacturing.

You will perform machine set-ups, troubleshoot production issues, maintain accurate documentation, and support continuous improvement initiatives within a structured production environment.

Key responsibilities: operate and monitor semi-automated production and packaging lines; perform machine set-ups, changeovers, line clearances, and cleaning activities; troubleshoot equipment and process issues and perform minor machine adjustments; record production activities and batch data in SAP and MES systems; support deviation investigations and production triage activities; contribute to Lean and Continuous Improvement initiatives; ensure compliance with GMP, safety, and quality standards; follow SOPs and work instructions to maintain efficient production; support optimal equipment performance and production reliability.

Requirements: MBO degree or equivalent technical background; experience operating production, assembly, labeling, or packaging equipment; technical understanding of manufacturing processes and equipment; strong analytical and troubleshooting skills; experience with Root Cause Analysis (RCA), 5 Why, or similar methodologies is an advantage; experience working within GMP or another regulated manufacturing environment; experience with SAP and/or MES systems; knowledge of Lean or Continuous Improvement methodologies is a plus; proactive, accurate, and quality-focused; fluent in English; willing to work in 3-shift and future 5-shift rotations.

Contract details: full-time position, competitive salary with shift allowances, learning and career development opportunities, modern GMP manufacturing environment with strong focus on employee well-being.

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