CQV Engineer — Pharma Commissioning Lead (Solid Dosage)

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

Job summary

Life Science Recruitment is recruiting for a CQV Engineer in Athlone to lead commissioning, qualification and validation activities for solid dosage equipment. You will manage CQV strategy, schedule, and documentation on client-side projects, ensuring risk-based verification and regulatory alignment.

The role requires at least 7 years' pharma commissioning experience, strong leadership of commissioning partners, and ability to present to senior governance forums while ensuring GMP/compliance

Qualifications

• Degree in Engineering or Science or related field.
• Minimum 7 years' GMP experience in pharma commissioning.
• Proven track record delivering CQV for solid dosage processes.
• Strong stakeholder management and reporting to senior leadership.

Responsibilities

• Develop and own CQV activities for projects, aligned to GMP requirements.
• Act as Client C&Q Lead, coordinating commissioning & qualification interfaces.
• Plan and lead system commissioning and qualification per project schedule.
• Oversee commissioning partners and sub-contractors to meet scope and program.
• Interface with QA, Manufacturing, EHS and QC; manage risk and documentation.

Skills

CQV Expertise

GMP Knowledge

CSV Fundamentals

Stakeholder Mgmt

Education

Engineering degree

Job description

Life Science Recruitment is recruiting for a CQV Engineer in Athlone to lead commissioning, qualification and validation activities for solid dosage equipment. You will manage CQV strategy, schedule, and documentation on client-side projects, ensuring risk-based verification and regulatory alignment.

The role requires at least 7 years' pharma commissioning experience, strong leadership of commissioning partners, and ability to present to senior governance forums while ensuring GMP/compliance