CQV Engineer - Life Sciences GMP Specialist (Relocation)

Adryan B.V; Schweiz; Vor Ort; EUR 96.763 - 129.018; Vollzeit

Benefits dieser Stelle

Relocation arrangement for non-Swiss

Employee benefits program

Public transportation pass

Zusammenfassung

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.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

MS Office

GMP knowledge

CQV experience

Communication skills

Team player

Customer oriented

Ausbildung

Bachelor's degree in engineering/science

Jobbeschreibung

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.