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QA Supervisor Leiden MY Recruitment

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Gevraagd

  • 37 - 40 uur
  • Medior/Senior
  • Nederlands (taal)

Aanbod

  • Vast contract
 

Vacature in het kort

Leiden
As a QA Supervisor, you'll lead a dynamic team of five in a hands-on role, ensuring seamless task coordination and active participation. Your leadership extends to staff development, equipment management, and process optimization using Lean principles. You'll oversee GMP compliance and manage audits, all while working in a diverse, international environment. This role promises an engaging mix of leadership and technical challenges within a vibrant industry. Continue on to see how this opportunity can transform your career.
 

Over het bedrijf

MY Recruitment
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Bedrijfsprofiel
 

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Korte omschrijving
One of your main goals is to ensure everything is well-organized for your team. As QA Supervisor you thrive in a dynamic environment with a variety of tasks.

Functie omschrijving

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.
     
Profiel kandidaat
  • Minimum of a Bachelor's degree level of education
  • Demonstrated experience in a QA or QC 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
Bedrijfsprofiel
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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