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QA Supervisor

Den Haag

Job description

As QA Supervisor you will be a hands-on leader within your team (5 fte). This means you will coordinate tasks within the group while also performing some of these tasks yourself. In this role, you will provide direction and guidance to your team and report directly to the QA Manager. Your responsibility will be:

Work Coordination: Distribute tasks, set work agreements, and monitor progress.
Staff Development: Conduct staff interviews in consultation with the QA Manager.
Equipment and Facilities: Release equipment, facilities, and utilities.
Process Optimization: Improve QA Systems processes using Lean principles, considering the interests of other departments.
Compliance: Supervise the implementation of GMP regulations and procedures.
Audit Coordination: Manage back-office operations during client audits and authority inspections.

Requirements

  • Minimum of a Bachelor's degree level of education
  • Demonstrated experience in a QA role within a GXP environment, preferably in a supervisory or coordinating capacity
  • Experience in a pharmaceutical, biotechnological, or service laboratory setting is preferred
  • In-depth knowledge of pharmaceutical quality systems

Company profile

Our client is a GMP contract service organization, specialized in chemical and physical testing and is part of an internationally operating Group. The laboratory performs a very diverse package of analyses of raw materials and finished products for a large number of national and international clients within the pharmaceutical industry.

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