Production Process Operator (Pharma)
SIRE® Life Sciences
Production Process Operator (Pharma)
Samenvatting
Wat krijg je?
Wat ga je doen?
- Bedienen van farmaceutische productielijnen conform GMP
- Monitoren van productieprocessen en afwijkingen melden
- Zorgen voor accurate documentatie en overdracht
- Identificeren van procesoptimalisaties voor continue verbetering
Wat verwachten wij?
- MBO level 2 education in technical production concepts
- 1-2 years experience in a manufacturing environment
- Knowledge of GMP, GDP, and SOP principles
- Experience operating pharmaceutical production lines
Volledige vacaturetekst
Support pharmaceutical production at a leading manufacturing company where safety and quality are central. You will operate automated lines in a dynamic environment, ensuring every health product meets strict GMP standards. Joining this diverse team means contributing to continuous improvement while enjoying a professional atmosphere. Ready to advance your career in a structured, high-tech setting? Take the next step and discover how you can impact global health.
The Company
Our client is a leading company in the pharmaceutical manufacturing sector, committed to delivering high-quality health products. They operate in a dynamic environment that emphasizes safety, quality, and continuous improvement. The organization values teamwork, professionalism, and adaptability among its diverse workforce.
About the Role:
An Associate Manufacturing Process Technician supports pharmaceutical production by operating automated, semi-automated, or manual manufacturing lines in compliance with GMP and standard operating procedures. The role requires maintaining a strong focus on safety, quality, efficiency, and delivery while meeting defined production targets in a shift-based environment.
Responsibilities:
- Operate pharmaceutical production lines in compliance with GMP, SOPs, and safety standards to meet quality and output targets.
- Monitor production processes, identify deviations, and escalate issues to the Line Lead in a timely and factual manner.
- Ensure accurate execution of standard work, documentation, and shift handover activities to maintain continuity and performance.
- Collaborate with team members across shifts and cultural backgrounds to achieve safety, quality, delivery, and efficiency goals.
- Contribute to continuous improvement by identifying process optimization opportunities and maintaining a disciplined, accountable work approach.
Requirements:
- 1-2 years of experience in a manufacturing environment, preferably in pharmaceutical, GMP, or regulated production settings.
- Education at MBO Level 2 (or equivalent), with a solid understanding of basic technical and production concepts.
- Knowledge of GMP/GDP, SOPs, and standard work principles within a structured manufacturing environment.
- Good English proficiency (reading, writing, and speaking) to communicate effectively in a multicultural workplace.
- Strong soft skills, including teamwork, flexibility, accountability, structured working style, and a continuous improvement mindset.
Other Information:
Looking for a new opportunity? Well, it's right here! If you're interested, please click the below button to apply for the job.
57330
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