Manufacturing Process Technician
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Manufacturing Process Technician gezocht voor semi-geautomatiseerde productielijnen in GMP-omgeving in Breda.
- Locatie
- Breda
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Sluitingsdatum
- Eerste waarneming
- Uitgezet via
- SIRE Life Sciences
Signalen van een warme stoel: Open, generic role for a manufacturing technician with clear requirements but no rate, no deadline, and no distinctive factors, making it average in appeal.
Dit is een inschatting op tekstkenmerken, geen bewijs. Zo werkt de warme stoel check.
Eisen
- Experience working with Standard Operating Procedures
- Able to work in a flexible, shift-based schedule
- Structured, accurate, and quality-oriented in work
- 2+ years of experience in a regulated manufacturing or packaging environment (GMP/GDP)
- Strong team player with a responsible and proactive attitude
- Good command of English (verbal and written)
Omschrijving
Company A leading global biotechnology organization dedicated to discovering, developing, and delivering innovative medicines for patients with serious illnesses. Driven by science and powered by advanced technology, the organization focuses on areas such as oncology, cardiovascular disease, inflammation, and rare diseases. Its mission is centered on improving lives by turning cutting-edge science into meaningful therapies that address unmet medical needs.
Job Description As a Manufacturing Process Technician you will be support the operation of semi-automated production lines within a GMP-compliant environment, ensuring efficient and accurate delivery of production targets across various shifts.
Responsibilities - Operate on packaging or assembly lines in accordance with standard operating procedures, ensuring product quality and safety (folding boxes, applying labels, etc.) - Collaborate closely with colleagues and line leads to meet daily production goals - Escalate issues or deviations clearly and promptly to the line lead. - Take ownership of assigned tasks, follow procedures diligently, and escalate when necessary - Participate actively in shift handovers, ensuring seamless communication between teams - Complete all required training and certifications on time - Adhere to safety, quality, and productivity standards during all shifts
Requirements - 2+ years of experience in a regulated manufacturing or packaging environment (GMP/GDP) - Experience working with Standard Operating Procedures - Good command of English (verbal and written) - Able to work in a flexible, shift-based schedule - Strong team player with a responsible and proactive attitude - Structured, accurate, and quality-oriented in work
Other Information Apply to our vacancy for more information. Looking forward to getting in touch!
Alle opdrachtenBekijk en reageer bij SIRE Life Sciences B.V. (externe link)
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