Senior CQV Manager for GMP Life Sciences

Adryan B.V; Netherlands; Remote; EUR 90,000 - 140,000; Part time

Benefits offered by this job

Company car

Laptop

Telephone

Personal training budget

Job summary

Adryan B.V. is recruiting a CQV manager for the Dutch life sciences market. You will lead a project team responsible for commissioning, qualification and validation of GMP facilities and equipment, and critical building and utility systems within our client’s life sciences production facility.

The role requires 10+ years in GMP environments, CQV expertise, and strong leadership. You will coordinate with clients and internal stakeholders to deliver compliant, timely CQV documents and build robust

Qualifications

• Bachelor’s or master's degree in engineering, science or related technical field or equivalent experience (HTS/TU in chemical/mechanical engineering).
• Proficient with MS Office; solid understanding of controlled documentation and data systems.
• In-depth knowledge of cGMP regulations.
• 10+ years in a GMP environment, preferably biotech.
• 8+ years CQV experience.
• 5+ years supervisory experience.
• Fluent in English and Dutch.

Responsibilities

• Develop and lead the CQV project team according to schedule and timelines.
• Ensure the CQV team provides timely, high-quality support.
• Maintain overview of all deliverables across project phases.
• Oversee design, IQ, OQ, PQ, IOQ documentation and validation reports.
• Represent Adryan to clients and stakeholders as SPC, coordinating responses.

Skills

Communication skills

Interpersonal skills

English language

Dutch language

Leadership

Problem-solving mindset

Customer focus

Supervisory experience

Education

Bachelor's or Master’s in engineering/science

HTS/TU in chemical/mechanical eng

Tools

MS Office

Document management systems

Job description

Adryan B.V. is recruiting a CQV manager for the Dutch life sciences market. You will lead a project team responsible for commissioning, qualification and validation of GMP facilities and equipment, and critical building and utility systems within our client’s life sciences production facility.

The role requires 10+ years in GMP environments, CQV expertise, and strong leadership. You will coordinate with clients and internal stakeholders to deliver compliant, timely CQV documents and build robust