Labeling Operator

SIRE LIFE SCIENCES

Breda

On-site

EUR 29,000 - 36,000

Full time

4 days ago
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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

Company

A leading biopharmaceutical manufacturing site is expanding its operations team to support high-quality production in a regulated environment. The organization works to strict quality and safety standards, values teamwork and continuous improvement, and operates within a diverse, international workplace where clear communication and professionalism are essential.

Job Description

We are looking for Labeling Operator to support day-to-day production activities within a GMP environment. The Biopharmaceutical Manufacturing Technician will work across multiple production lines (automated, semi-automated, and manual) and help ensure that safety, quality, and output targets are consistently met.

Responsibilities
  • Operate production equipment and run manufacturing processes in line with approved - procedures and standard work.
  • Support safe and compliant execution of activities, ensuring quality and documentation standards are followed.
  • Collaborate closely with other operators and the line lead to deliver daily production targets.
  • Escalate deviations, issues, or safety/quality concerns clearly and promptly, using factual communication.
  • Contribute to shift handovers to ensure smooth continuity of work and clear status updates.
  • Identify and suggest improvements to enhance efficiency, reliability, and ways of working.
  • Take ownership of assigned tasks, training obligations, and results, demonstrating accountability and maturity.
  • Remain flexible to switch between lines and tasks based on operational priorities.
Requirements
  • 1–2 years of experience in a manufacturing environment (pharmaceutical/GMP experience preferred).
  • Comfortable working with standard operating procedures 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, learning mindset, and openness to change and continuous improvement.
  • Education level comparable to vocational training (MBO level 2 or similar).
  • This is a 2 or 3 shift position
Other Information

This position is based on-site in the Breda area and involves working in a professional production setting with clear performance expectations around safety, quality, delivery, and efficiency.

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