Job Description

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Commissioning, qualification & validation engineer

Adryan is an internationally operating services group with offices in The Netherlands and Switzerland, offering services for the life sciences industry, specializing in project management, engineering, CQV, and compliance.

As a hands-on CQV engineer, you will be part of a project team responsible for commissioning, qualification, and validation activities of GMP facilities, process equipment, and critical systems within our client’s life sciences production facility. This includes designing, implementing, and documenting qualifications and lifecycle management in compliance with regulatory standards (FDA and EU).

Key responsibilities:

  • Accountable for all CQV activities within project timelines.
  • Providing support efficiently and with high quality.
  • Designing, developing, executing...

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