CQV Engineer - Pharma Equipment Commissioning Lead

Life Science Recruitment; Athlone; On-site; EUR 90,000 - 120,000; Full time

Job summary

Life Science Recruitment is seeking a CQV Engineer in Athlone for a leading pharmaceutical organisation. You will lead CQV activities, ensuring commissioning and qualification meet GMP standards and project timelines.

You will coordinate with Quality, Manufacturing and Engineering, manage CQV risks, and drive successful handover to operations with complete documentation and training where required.

Qualifications

• Degree qualification in Engineering, Science, related discipline or relevant experience.
• Pharma GMP experience in manufacturing environments.
• Minimum 7 years’ GMP experience, with demonstrable experience.
• Proven track record of commissioning and qualification of solid dosage equipment.
• Experience planning and delivering complex commissioning and qualification of systems.
• Excellent stakeholder management and reporting skills to senior leadership.

Responsibilities

• Develop and own CQV activities aligned to project schedule and GMP requirements up to PQ of all systems.
• Act as Client CQV Lead and coordinate all commissioning/qualification activities.
• Plan and lead system commissioning and qualification with phased area releases.
• Oversee commissioning partners and subcontractors, managing scope and programme.
• Interface with Quality, Manufacturing, Operational Readiness, Engineering, EHS, QC.
• Provide CQV status reporting to Senior Project Manager; manage risk registers.

Skills

CQV leadership

GMP experience

Stakeholder management

Risk management

Qualification documentation

Project coordination

Education

Engineering/Science degree

Job description

Life Science Recruitment is seeking a CQV Engineer in Athlone for a leading pharmaceutical organisation. You will lead CQV activities, ensuring commissioning and qualification meet GMP standards and project timelines.

You will coordinate with Quality, Manufacturing and Engineering, manage CQV risks, and drive successful handover to operations with complete documentation and training where required.