Careers

Technical collaboration for regulated projects.

We have no specific vacancy at present. We welcome contact with experienced professionals who know quality management, qualification, validation or CSV from practical work.

Current opportunities

No current vacancies

We will publish new positions and application information here when we expand our team.

Interested in QMVP?

Please check back later or explore how we work and our technical areas of expertise.

Your profile

The expertise you bring

QMVP may be a good fit if you know regulated environments from practical experience and want to contribute independently to quality management, qualification, validation or CSV projects.

Several years of project experience in GxP-regulated environments (pharma, medical devices, biotech)
In-depth expertise in at least one area: quality management, CQV or CSV/GAMP 5
Independent working and direct communication with clients
Enjoyment of practical project work rather than internal processes

Collaboration

What to expect at QMVP

You work in a small, experienced team with direct technical coordination, clear responsibilities and a close connection to practical project delivery.

Technically demanding projects in regulated environments
Direct coordination without unnecessary handovers
Flexible, project-based work
Space to shape project approaches with your experience

Get in touch about working together

Would you like to work with QMVP?

Even without an advertised vacancy, you can send us a brief message about your technical focus and project experience. We will assess whether there is a suitable opportunity to collaborate.

Introduce your profile

Learn how we process applicant data in the section Applicant privacy.