Location: Nijmegen – The Netherlands
Work model: On-site
Employment type: Full-time

About the role

For a regulated MedTech production environment in the Nijmegen region, we are looking for a hands-on and quality-minded Production Operator.

In this role, you support controlled production activities for an innovative product used by patients worldwide. Accuracy, safety and working according to clear procedures are essential.

You will perform production steps in line with GxP guidelines and ensure that your work is carried out and documented correctly. This is a practical role for someone who takes ownership, works carefully and understands that every step in the production process matters.

Key responsibilities

  • Manufacture products according to procedures, Good Manufacturing Practices, Good Documentation Practices and applicable quality standards.
  • Prepare and complete documentation for the various manufacturing steps.
  • Prepare and verify batch components.
  • Perform product quality inspections according to specifications.
  • Clean the work area to prevent contamination and product mix-ups.
  • Follow written procedures accurately and consistently.
  • Work in compliance with safety, quality and GxP/GMP requirements.
  • Communicate clearly with colleagues about production progress, deviations or points of attention.
  • Contribute to a clean, organised and inspection-ready production environment.

Requirements

You are accurate, practical and quality-minded. You understand the importance of following procedures carefully in a regulated production environment and you take responsibility for correct execution and documentation.

You enjoy hands-on work, communicate clearly and are willing to learn new processes.

Your background

  • MLO degree with relevant experience, or an HBO degree as a starter.
  • Experience in a production or laboratory environment.
  • Experience in a pharmaceutical, MedTech or other regulated environment is preferred.
  • Knowledge of GxP, GMP or working according to strict procedures is a plus.
  • Accurate, detail-oriented and able to follow written procedures carefully.
  • Comfortable working in a team and communicating clearly.
  • Flexible, hands-on and eager to learn new processes.
  • Fluent in English, both spoken and written.

What you can expect

You will work in an international, quality-driven MedTech production environment where accuracy, safety and compliance are central.

The role offers hands-on production work, responsibility and the opportunity to contribute to products that support patients worldwide. You can expect specialist training, development opportunities, good employment conditions and a collaborative working environment.

Job category: Operations
Job type: Full-Time
Job location: Nijmegen - The Netherlands

Reageer op deze functie

Toegestane typen: : .pdf, .doc, .docx