Technical Operator - Semi-Automated Lines
SIRE® Life Sciences
Technical Operator - Semi-Automated Lines
Samenvatting
Wat krijg je?
Wat ga je doen?
- Operate semi-automated production lines
- Perform machine set-ups and changeovers
- Troubleshoot equipment and process issues
- Record data in SAP and MES
- Support investigations and production triage
Wat verwachten wij?
- MBO opleiding in een technische richting
- Ervaring met het bedienen van productie- en verpakkingsmachines
- Technisch inzicht in productieprocessen en apparatuur
- Ervaring met werken in een GMP-omgeving
Volledige vacaturetekst
Join a leading international pharmaceutical manufacturer as a Technical Operator for semi-automated lines. In this GMP-regulated environment, you will monitor production equipment and solve technical challenges to ensure global distribution of vital medicines. You will work in a modern facility that prioritizes employee well-being and offers excellent learning opportunities for career growth. Discover how you can impact global health and apply today!
About the Company
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.
Role Description
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
- 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
- Full-time position
- Competitive salary with shift allowances
- Learning and career development opportunities
- Modern GMP manufacturing environment with strong focus on employee well-being
59030
Over de werkgever
Zo werkt solliciteren
- Snel en eenvoudig via je mobiel
- Solliciteer in 1 minuut
- CV niet verplicht
- Volg je sollicitatie via Track & Trace
- Volg je sollicitatie via Track & Trace
Goed om te weten
Makkelijk solliciteren Solliciteren
