Labeling Operator
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Labeling Operator in Breda voor een biopharmaceutical manufacturing site, op locatie, tijdelijke functie, 2- of 3-shift.
- Locatie
- Breda
- Werkvorm
- op locatie
- Uren
- 20–24 uur per week
- Contractvorm
- zzp
- Startdatum
- Sluitingsdatum
- Gepubliceerd
- Uitgezet via
- SIRE Life Sciences
Eisen
- Goede beheersing van het Engels (mondeling en schriftelijk)
- 1-2 jaar ervaring in een productieomgeving
- Comfortabel met standaardwerkprocedures en gestructureerde werkwijzen
- Teamgericht, betrouwbaar en nauwkeurig werken
- Proactieve houding, leergierigheid en openheid voor verandering en continue verbetering
- Opleidingsniveau vergelijkbaar met MBO niveau 2 of hoger
- Flexibele instelling en bereidheid om in verschillende ploegendiensten te werken
Wensen
- Farmaceutische/GMP-ervaring
Omschrijving
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. 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. If you are interested and want to apply, please submit your application via the apply button below and contact me.
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