Quality Manager with focus on software validation (m/f/d)

To support our Quality Management department in Hamburg, we are looking for a highly motivated and committed Quality Manager with focus on software validation (m/f/d)



Your responsibilities

  • Implementation of quality requirements according to EN ISO 13485 and the Medical Device Single Audit Program (MDSAP) as well as according to requirements from other national and international standards, laws and guidelines for in-vitro diagnostics
  • Monitoring of the introduction of a document management system and support of the specialist departments
  • Planning, support and implementation of software validation projects
  • Support in the implementation of the company-specific quality policy and quality objectives
  • Implementation, support, and follow-up of internal and external audits


Your expertise

  • Successfully completed studies / training or comparable qualification
  • Knowledge in the field of process and software validation
  • Ability to understand standards and laws, and ability to consider and establish them in processes
  • Sound MS Office skills
  • Very good knowledge of German and English, both written and spoken
  • A high degree of initiative and sense of responsibility for the assigned tasks/projects
  • Strong communication and coordination skills

Our offer

Benefit from a wide range of opportunities available within an expanding international company. You will work both independently and as part of a team in a highly motivated, open, and friendly environment. Family-friendly working hours along with a pleasant and familial working atmosphere await you.

Are you interested?

Then we are looking forward to receiving your detailed application including your availability and salary expectations. Please send us your complete application documents (ideally in PDF format) using the “Apply now” button. Your contact person is Ms. Dina Jensen.



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Quality Manager with focus on software validation (m/f/d)

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Thank you very much for your interest in joining our company.

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