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Quality Engineer Amsterdam Talentmark

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Gevraagd

  • Fulltime
  • Engels (taal)

Aanbod

  • Loondienst (vast)
  • 3.900 - € 5.000 p/m (bruto)
 

Vacature in het kort

Amsterdam
Join a dynamic team as a Quality Engineer, where you'll play a pivotal role in supporting quality across various production departments. Dive into inspections, lead investigations, and drive quality improvements to enhance departmental processes. Contribute to value stream management and ensure timely product releases. Enjoy the benefits of extra training programs to further develop your skills and ensure compliance with the highest industry standards. Take the next step and explore why this role is a great fit for you.
 

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Talentmark
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Quality Engineer – Amsterdam

As a Quality Engineer, you will be the first point of contact for quality support across several production departments. Your responsibilities will focus on inspections, investigations, reporting, and advising on and implementing quality improvements. The main objective of your role is to safeguard and optimize the continuity and quality of departmental processes. You will operate within a matrix organization, contributing to value stream management across multiple products and ensuring release timelines are met.

Key Responsibilities

  • Identify opportunities for improvement and implement necessary changes
  • Lead quality investigations for products and/or services within production
  • Ensure compliance with GxP guidelines
  • Perform internal quality controls and inspections on processes, activities, and services
  • Oversee, evaluate, and coordinate routine validations
  • Translate data and findings from inspections, investigations, and validations into clear, insightful reports for senior management


About the company
The company is one of the few end-to-end pharmaceutical companies in the Netherlands. Our production process covers every stage, from raw material to the final filled and packaged product, adhering to the highest GMP standards. Quality and safety are regularly inspected and validated by both Dutch and international regulatory authorities.

Your Profile

  • Bachelor’s degree in a scientific field, with knowledge of quality processes in pharmaceutical production
  • Work experience in the pharmaceutical industry
  • Strong knowledge of GxP guidelines and relevant software systems
  • Experience with automation and/or engineering in a production setting
  • Excellent analytical and communication skills
  • Comfortable working in a matrix organization
  • Experience on writing investigations is a must
  • Curious about developments in your field and eager to advise on their applicability in production
  • Proficiency in English, both written and spoken
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