CQV Manager – Pharmaceutical Facility (Frankfurt, Germany)

We are looking for an experienced CQV Manager to join a major pharmaceutical facility project in Frankfurt, Germany. This is a full-time, on-site role within a highly regulated GMP environment, supporting the delivery of a large-scale capital project in close coordination with Construction, Engineering, QA, and Project Controls teams.

The ideal candidate has solid experience in Commissioning, Qualification & Validation for pharmaceutical or biotech facilities and is comfortable leading multidisciplinary teams through all CQV phases.

Key Responsibilities

• Lead and oversee all CQV activities across systems (utilities, clean utilities, HVAC, process equipment, automation, and related subsystems).

• Develop and manage CQV strategies, plans, schedules, protocols (IQ/OQ/PQ), and documentation in alignment with project and regulatory requirements.

• Coordinate with Engineering, Construction, QA, and Operations to ensure readiness for commissioning, qualification, and handover.

• Ensure compliance with GMP, GEP, and applicable regulatory guidelines throughout the project lifecycle.

• Identify risks, deviations, and blockers, proposing mitigation strategies and ensuring timely resolution.

• Manage vendors, supervise execution of protocols, and ensure alignment of all involved stakeholders.

Provide clear reporting to project leadership and support decision-making with data-driven insights.

Requirements

• Proven experience as a CQV Manager or senior CQV professional in pharmaceutical or biotech facility projects.

• Strong knowledge of GMP, GEP, validation lifecycle, and regulatory expectations (FDA/EU).

• Experience working on large capital projects (utilities, clean rooms, process equipment)

• Familiarity with integrated project environments and multidisciplinary coordination.

• Fluency in German (mandatory) and very good command of English.

• Availability to start as soon as possible.

Ability to work full-time on site in Frankfurt.

How to Apply

If you meet the above criteria and are interested in joining this high-impact project, please submit your application and attach your CV in English.

We look forward to hearing from you.

Pharmatec SRL is an equal opportunity employer. We welcome applications from all qualified individuals, regardless of race, color, religion, gender, sexual orientation, gender identity, nationality, or disability.