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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, and archiving CQV documentation, including IQ, OQ, PQ protocols, and reports according to industry standards.
Analyzing validation data and summarizing findings.
Identifying GMP requirements during design validation.
Resolving discrepancies and planning follow-up actions.
Making recommendations on test strategies.
Conducting and coordinating validation testing.
Maintaining good team communication and troubleshooting.
Job Requirements: Bachelor’s degree in engineering, science, or related field (e.g., chemical or mechanical engineering).
Proficient with MS Office and data systems.
Deep knowledge of cGMP regulations.
5+ years GMP experience, preferably in life sciences.
3+ years CQV experience.
Flexible, solution-oriented team player with positive attitude.
Customer and result-focused with good communication skills.
Job offer: Challenging role in a growing organization.
Engaging projects within the life sciences network.
Attractive salary based on experience.
Social contributions, Swiss public transport pass, training budget, employee benefits, knowledge sharing, relocation support for non-Swiss candidates, team events, and a supportive team environment.
If interested, apply for the CQV Engineer position.
Details: Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Engineering and IT
Industry: Pharmaceutical Manufacturing
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