Production Line Operator
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Manufacturing Technician vacancy at a global biotech in Breda, operating GMP production lines, shift work, English required, start 6/10/2026.
- Locatie
- Breda, Noord-Brabant
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
- Opdrachtgever
- unnamed client
Eisen
- Good communication skills in English (verbal, reading, writing)
- Ability to work in a team-oriented, multicultural environment
- Flexibility to work in different shift patterns as needed
- 1+ years of experience in a manufacturing environment, preferably in GMP-regulated pharmaceutical or similar industries
- Strong understanding of standard operating procedures and productivity principles
- MBO level (level 2) education or equivalent
Omschrijving
The client is a leading global biotechnology organization dedicated to developing and delivering innovative medicines to improve patient outcomes. Operating worldwide, the company combines science, technology, and quality-driven processes to ensure safe and effective clinical products. We are seeking a dedicated and motivated Manufacturing Technician to join our client's production team in Breda, Noord-Brabant. This role involves operating and maintaining production lines within a fast-paced pharmaceutical environment, ensuring that all processes adhere to strict GMP standards. The technician will collaborate closely with team members to meet production goals and uphold safety and quality standards. Responsibilities include operating production lines in accordance with detailed operating procedures, ensuring products are manufactured safely and efficiently; communicating effectively with team members and line leads to achieve daily production targets; identifying opportunities for process improvements and supporting initiatives to enhance efficiency and quality; escalating issues or deviations promptly to the line lead, maintaining clear and factual reporting; taking ownership of assigned tasks and ensuring all activities are completed accurately and on time; participating actively in shift handovers and ensuring proper documentation of tasks and results; and following all training requirements and maintaining up-to-date knowledge of production processes. Requirements: 1+ years of experience in a manufacturing environment, preferably in GMP-regulated pharmaceutical or similar industries; strong understanding of standard operating procedures and productivity principles; good communication skills in English (verbal, reading, writing); ability to work in a team-oriented, multicultural environment; flexibility to work in different shift patterns as needed; MBO level (level 2) education or equivalent. Job reference 58182. Sector: Pharmaceuticals.
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