GMP Labeling Technician

SIRE LIFE SCIENCES; Breda; On-site; EUR 29,000 - 36,000; Full time

Job summary

SIRE LIFE SCIENCES in the Breda area is seeking a Labeling Operator to support day-to-day production in a GMP environment. The Biopharmaceutical Manufacturing Technician will work across multiple production lines (automated, semi-automated, and manual) and help ensure safety, quality, and output targets are met.

You should have 1–2 years in manufacturing (pharma/GMP preferred), be comfortable with SOPs, and communicate effectively in English in an international setting.

Qualifications

• 1–2 years manufacturing experience, GMP/pharma experience preferred.
• Comfortable with SOPs and structured ways of working.
• Good command of English (verbal and written) in an international environment.
• Team oriented, reliable, and able to work accurately at a consistent pace.
• Flexible mindset and willingness to work in different shift patterns.
• Proactive attitude and openness to change and continuous improvement.

Responsibilities

• Operate production equipment and run manufacturing processes per approved procedures and standard work.
• Support safe and compliant execution of activities, ensuring quality and documentation standards.
• Collaborate with operators and line lead to meet daily production targets.
• Escalate deviations, issues, or safety/quality concerns clearly and promptly.
• Contribute to shift handovers for smooth continuity and clear status updates.
• Identify and suggest improvements to enhance efficiency and reliability.
• Take ownership of assigned tasks, training obligations, and results.
• Remain flexible to switch between lines and tasks based on priorities.

Education

MBO level 2 or similar

Job description

SIRE LIFE SCIENCES in the Breda area is seeking a Labeling Operator to support day-to-day production in a GMP environment. The Biopharmaceutical Manufacturing Technician will work across multiple production lines (automated, semi-automated, and manual) and help ensure safety, quality, and output targets are met.

You should have 1–2 years in manufacturing (pharma/GMP preferred), be comfortable with SOPs, and communicate effectively in English in an international setting.