Manufacturing Process Technician
SIRE® Life Sciences
Manufacturing Process Technician
Samenvatting
Wat krijg je?
Wat ga je doen?
- Operate packaging and assembly lines
- Escalate production issues and deviations
- Participate in daily shift handovers
- Maintain safety and quality standards
- Complete required training and certifications
Wat verwachten wij?
- Twee jaar ervaring in een GMP-productieomgeving
- Ervaring met het werken volgens Standard Operating Procedures
- Ervaring met het bedienen van verpakkings- en assemblagelijnen
- Teamplayer, flexibel, communicatief
Volledige vacaturetekst
Support the operation of semi-automated production lines at a leading global biotechnology organization dedicated to innovative medicines. In this role, you contribute to life-saving therapies within a GMP-compliant environment. You collaborate with a driven team to ensure high-quality standards in oncology and rare diseases. Experience the impact of cutting-edge science firsthand while enjoying a dynamic atmosphere. Dive into the future of medicine and make a real difference today!
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
- 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
Apply to our vacancy for more information. Looking forward to getting in touch!
57850
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