CQV Lead: Pharma Equipment Commissioning & Qualification

DPS Group Global; Athlone; On-site; EUR 90,000 - 130,000; Full time

Job summary

DPS Group Global is seeking an experienced SRV ER to lead CQV activities for pharma Process Equipment in a solid dosage environment. The role is client-side, reporting to the SRV supervisor, and will oversee commissioning strategy, schedule, quality, safety and compliance across the CQV lifecycle.

Candidates should bring 5+ years of GMP pharma commissioning experience, strong leadership, and a proven ability to manage commissioning partners and contractors to ensure timely, compliant delivery.

Qualifications

• Minimum 5+ years GMP experience in pharma commissioning.
• Experience with solid dosage process equipment installation.
• Proven track record in commissioning and qualification of complex systems.

Responsibilities

• Own CQV activities aligned to project schedule and GMP requirements.
• Coordinate commissioning and qualification with CQV interfaces.
• Plan and lead system commissioning and qualification for equipment.
• Interface with Quality, Manufacturing, EHS, QC.
• Provide CQV status reports to the Senior Project Manager.
• Manage risk, deviations and change controls.
• Ensure documentation and handover to CQV and Operations.

Skills

Leadership

Stakeholder management

Problem solving

Communication

Education

Degree qualification in Engineering or Science

Job description

DPS Group Global is seeking an experienced SRV ER to lead CQV activities for pharma Process Equipment in a solid dosage environment. The role is client-side, reporting to the SRV supervisor, and will oversee commissioning strategy, schedule, quality, safety and compliance across the CQV lifecycle.

Candidates should bring 5+ years of GMP pharma commissioning experience, strong leadership, and a proven ability to manage commissioning partners and contractors to ensure timely, compliant delivery.