CQV Engineer - Life Sciences GMP Specialist (Relocation)

Adryan B.V

Schweiz

On-site

EUR 96,763 - 129,018

Full time

14 days+

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Benefits offered by this job

Relocation arrangement for non-Swiss

Employee benefits program

Public transportation pass

Job summary

Adryan is recruiting a hands-on CQV engineer to join our project team for the Swiss and Western European life sciences market. You will lead commissioning, qualification and validation activities for GMP facilities and critical systems, ensuring documentation and regulatory compliance.

The role requires a Bachelor in engineering or science, 5+ years GMP experience, 3+ years CQV, and strong communication and teamwork.

Qualifications

Bachelor’s degree in engineering, science or related technical field (e.g., ETH/EPFL).
Proficient with MS Office and controlled documentation/data systems.
5+ years of experience in a GMP environment (life sciences preferred).
3+ years of CQV experience.
Strong communication and teamwork skills.

Responsibilities

Accountable for all CQV activities as required by schedule and project timelines.
Provide support in a timely, efficient and quality manner.
Design, develop, execute, write and archive C&Q documentation (IQ/OQ/PQ) per standards.
Analyze validation data and summarize findings in final reports.
Identify GMP requirements for validation during design.
Resolve protocol/discrepancies and plan follow-ups.
Make recommendations on test strategies and approaches.
Coordinate validation testing and maintain team collaboration.