Production Quality Engineer and Consultant

1 week ago


Kongens Lyngby, Lyngby-Tårbæk Kommune, Denmark PharmaRelations ApS Full time

Company Overview:

PharmaRelations ApS specializes in medtech, veterinary diagnostics, and develops point-of-care instruments used in veterinary clinics and on farms.

We are a global market-leading company with strong core values regarding our workforce.

As a Quality Engineer Consultant, you will be responsible for key assignments such as CAPA process, validation, documentation, and case handling. This includes batch release and complaint handling.

The ideal candidate will have a natural interest in making QA a value-adding support for the business, mainly production, but also Engineering and R&D Projects. You will be responsible for developing and maturing the QA processes, particularly in complaint handling, deviation/CAPA, and batch release.

Major Accountabilities:
  • Develop and mature QA processes with specific focus on Complaint handling, Deviation/CAPA, and batch release.
  • Excel in communication and thrive as an ambassador for Quality in the organization.
  • Bring know-how and expertise to the full end-to-end process.
Education & Qualifications:
  • A degree in engineering or life sciences.
  • Working knowledge as QA for production and/or engineering.
  • Understanding of industry standards such as GMP or ISO.
  • Experience in working in the device or pharmaceutical industry.
  • You have a flair for various technical aspects in production and quality documentation systems.
  • Good communication capabilities.
  • You manage to work cross-functionally in an international setting and bring pragmatic solutions to the table in a vibrant work environment.


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