Manufacturing Technician

The company is a global biotechnology company dedicated to improving the lives of patients. In Breda they focus on preparing, planning, and coordinating the shipping and distribution of clinical trial materials. As a Production Operator on the manual packaging lines, you will perform hands-on production and packaging activities within a highly regulated pharmaceutical manufacturing environment. You will be responsible for executing tasks according to established procedures while ensuring the highest standards of quality, compliance, safety, and operational excellence.

This role requires strong attention to detail, a disciplined approach to following GMP requirements, and the ability to perform repetitive tasks consistently and accurately.

Responsibilities include: performing manual production and packaging activities in compliance with Standard Operating Procedures (SOPs); completing packaging operations accurately and according to approved processes; carrying out in-process quality inspections and checks; maintaining accurate GMP documentation, including batch records and production logs; identifying, reporting, and supporting the investigation and resolution of deviations or quality-related issues; participating in production triage and problem-solving discussions with Quality Assurance and Production teams; executing line set-up, changeover, and close-down activities; performing routine cleaning tasks; ensuring the production area remains safe, compliant, organized, and inspection-ready; consistently performing repetitive manual operations while maintaining quality and productivity standards; and collaborating effectively with colleagues.

Requirements: Minimum of 2 years' experience in a manufacturing, production, or packaging environment; MBO Level 2 qualification (or equivalent); previous experience within a regulated industry is preferred; basic understanding of GMP principles, SOPs, and manufacturing processes; experience working with ERP or manufacturing systems such as SAP or MES is advantageous; fluent in English, both written and spoken; strong attention to detail; ability to follow procedures precisely; good manual dexterity; reliable, accurate, and disciplined; strong compliance mindset; team-oriented; availability to work in a two-shift operation; comfortable performing repetitive manual production activities; and able to work in an environment where strict adherence to procedures and GMP requirements is essential.

Other information: Apply to our vacancy for more information.