Senior CQV Engineer – Solid Dosage Pharma (Client-Side)

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

Job summary

Life Science Recruitment is helping a leading pharmaceutical organization in Athlone find a CQV Engineer to drive commissioning, qualification and validation activities for solid dosage facilities. The role is client-side, focusing on commissioning strategy, schedules, quality and compliance throughout the CQV lifecycle.

The successful candidate will collaborate with Quality, Manufacturing, Operational Readiness, Engineering and EHS, ensuring GMP, CSV fundamentals and regulatory expectations are

Qualifications

• Minimum 7 years GMP experience in pharma commissioning.
• Experience commissioning and qualification involving solid dosage equipment.
• Strong project coordination with external partners and contractors.

Responsibilities

• Develop and own CQV activities aligned to project schedule and GMP requirements.
• Plan and lead system commissioning and qualification of equipment.
• Coordinate commissioning partners and sub-contractors across the project.
• Interface with Quality, Manufacturing, Engineering, and other stakeholders.
• Provide regular CQV status reporting and risk management updates.

Skills

CQV management

GMP experience

Stakeholder management

Regulatory knowledge

Education

Engineering/Science degree

Tools

CSV fundamentals

Job description

Life Science Recruitment is helping a leading pharmaceutical organization in Athlone find a CQV Engineer to drive commissioning, qualification and validation activities for solid dosage facilities. The role is client-side, focusing on commissioning strategy, schedules, quality and compliance throughout the CQV lifecycle.

The successful candidate will collaborate with Quality, Manufacturing, Operational Readiness, Engineering and EHS, ensuring GMP, CSV fundamentals and regulatory expectations are