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QA Officer GMP

For a growing pharmaceutical company in Flevoland, we are looking for an all-round QA Officer.

Job Description

As QA Officer GMP you will work in a small Quality Assurance team, which allows you to take on a lot of responsibility in an all-round position. Besides your standard activities (see below), the company is also working on the implementation of a new quality management system (QMS). You can contribute to this by assisting in the implementation and validation of the system, from start to finish. You will train colleagues and ensure the integration of the program within the company's working methods.

Responsibilities

  • Processing changes in (quality system) documentation
  • Checking batch documentation; batch review/release under GMP
  • Working together with and supporting the QA Manager for implementing of the QMS
  • Supporting other Quality processes as needed (CAPA's, changes, complaint handling, audits, etc.)

Profile

  • Completed HLO or HBO education in the field of life science or related topics
  • Experience with working under a Quality Management System (QMS) is a must
  • Experience with administrative work; this experience is preferably gained in a GMP environment
  • Independence, critical and accurate working
  • good communicative and social skills, team player
  • professional knowledge in Dutch and English (written and spoken)
  • Experience with Electronic Document Management Systems and Good Manufacturing Practices (GMP) is an advantage

Working conditions

  • Employment: view on permanent employment
  • Salary indication: €2600 to €3400 per month
  • Working hours: full-time (32 hours is negotiable)
  • Location: Flevoland
  • Vacancy number: 19746