Quality Engineer for Production

8 hours ago

LyngbyTaarbæk Kommune, Denmark PharmaRelations ApS Full time

PharmaRelations ApS

Denmark - Copenhagen

Apply now
On behalf of one of our medtech and diagnostics clients, we are looking for a talented Quality Engineer Consultant for production to ensure the site Quality Policy is understood, implemented, and maintained at all levels of the site organization.

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

The position is temporary for 6 months with the possibility for extension.

We are looking for a skilled and motivated Quality Engineer for production who has a natural interest in making QA a value-adding support for the business, mainly production, but also Engineering and R&D Projects.

You see this role as combining your interest to grow in a QA excellence department even further with the team. You will be responsible for key assignments such as CAPA process, validation, documentation, and case handling. This also includes batch release and complaint handling. You have a flair for various technical aspects in production and quality documentation systems and have a keen interest and experience with good communication capabilities.

Major Accountabilities
  • In the role as QA for production, it is vital that you can develop and mature the QA processes with specific focus on Complaint handling, Deviation/CAPA, and batch release.
  • You excel in communication and thrive with the role as “ambassador” for Quality in the organization.
  • With your experience from production within ISO-certified or regulated industries, you will 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.
Technical Skills Requirements
  • QMS systems skills.
  • Fluent in Danish and English.
  • Case handling.
  • Complaint handling.
  • Deviation/CAPA.
  • Batch release.
We offer

This is a unique and challenging job in a global market-leading company, where you will have opportunities to excel and expand your competencies together with highly skilled and committed colleagues.

You become part of an ambitious company with strong core values also regarding its workforce.

For further information, reach out to Farshin Simonsen, Head of Medical Interim on +45 54 33 44 13 or

Due to GDPR, we cannot receive any applications or CVs by mail. Interviews are already taking place, so please get in touch or apply at your earliest convenience.

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