Semi-Automated Lines Operator – GMP Production

SIRE LIFE SCIENCES; Breda; On-site; EUR 42,000 - 54,000; Full time

Benefits offered by this job

Shift allowances

Career development

GMP manufacturing environment

Job summary

SIRE LIFE SCIENCES is seeking a Technical Operator for semi-automated production lines in Breda. You will operate and monitor lines, perform set-ups, troubleshoot issues, and document batch data in SAP and MES within a GMP framework.

You will contribute to Lean improvements, follow SOPs, and support safe, efficient manufacturing in a 3- to 5-shift rotation environment. English fluency is required.

Qualifications

• 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 SAP and/or MES systems.
• Knowledge of Lean or Continuous Improvement methodologies is a plus.
• Fluent in English.

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.

Skills

Analytical skills

Troubleshooting

Root Cause Analysis

Lean/CI mindset

English fluency

Manufacturing equipment operation

Education

MBO degree or equivalent technical background

Tools

SAP

MES systems

Job description

SIRE LIFE SCIENCES is seeking a Technical Operator for semi-automated production lines in Breda. You will operate and monitor lines, perform set-ups, troubleshoot issues, and document batch data in SAP and MES within a GMP framework.

You will contribute to Lean improvements, follow SOPs, and support safe, efficient manufacturing in a 3- to 5-shift rotation environment. English fluency is required.