GMP Operator
GMP Operator for a regulated manufacturing client in Breda, temporary full-time contract (1 year), start 16 October 2026.
Bekijk bij SIRE Life Sciences B.V. (opent in een nieuw tabblad)
Eisen
- Good technical understanding and the ability to identify and solve production issues
- Technical education at MBO level or an equivalent qualification such as VAPRO B
- Available for a temporary full-time contract (1 year)
- Experience in automated production, assembly, packaging, or process manufacturing
- Knowledge of SAP, MES, or similar production systems
- Willingness to work rotating 3-shift and 5-shift schedules
- Good communication skills in English
Wensen
- Familiarity with RCA, 5 Why, Lean, or Kaizen
- Experience in GMP or another regulated manufacturing environment
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Volledige omschrijving
Company: Our client is an international manufacturing company operating in a highly regulated production environment. The organisation uses advanced automated manufacturing and packaging technologies to deliver high-quality products while maintaining strong standards for safety, compliance, and operational excellence. The site values teamwork, continuous improvement, technical expertise, and innovation.
Job Description: We are looking for a Manufacturing Operator to join a dynamic production team. In this role, you will help keep semi-automated production and packaging lines running safely, efficiently, and according to GMP requirements. You will monitor equipment, handle basic technical issues, complete production activities, and support the team in keeping production running smoothly.
Roles & Responsibilities: Run and monitor semi-automated production and packaging lines in a GMP environment. Set up and start production equipment according to SOPs and production instructions. Check and adjust machines and process settings when needed. Carry out cleaning, product changeovers, line clearance, and basic equipment checks. Identify and troubleshoot machine or process issues to reduce production downtime. Make basic machine adjustments to keep the production process running smoothly.
Record and verify production information in SAP, MES, and other manufacturing systems. Complete batch records, equipment logs, and other production documentation accurately. Check product quality during production and report deviations or abnormalities. Perform first-line checks and basic maintenance when required. Follow GMP, SOPs, safety rules, and site procedures at all times. Coordinate with Production, Maintenance, and Quality teams to resolve technical or production issues.
Support root cause investigations using methods such as 5 Why and RCA. Contribute to continuous improvement initiatives using Lean and Kaizen principles. Communicate clearly during shift handovers and share relevant production information with colleagues.
Requirements: Technical education at MBO level or an equivalent qualification such as VAPRO B. Experience in automated production, assembly, packaging, or process manufacturing. Good technical understanding and the ability to identify and solve production issues. Familiarity with RCA, 5 Why, Lean, or Kaizen is an advantage. Experience in GMP or another regulated manufacturing environment is highly desirable. Knowledge of SAP, MES, or similar production systems.
Good communication skills in English. Willingness to work rotating 3-shift and 5-shift schedules. Available for a temporary full-time contract (1 year). Why Apply? This role is a great opportunity for someone who enjoys working with modern manufacturing technology and solving technical production challenges. If you're ready for your next challenge in automated manufacturing, we'd love to hear from you. Apply today by clicking the application button below or contact me directly for more information.
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