CQV Engineer

Job description

PM Group is a leading International engineering, architecture, project and construction management firm. With a network of offices in Europe, Asia and the US and a multi-discipline team of over 3,700+ people. We deliver complex, capital projects in the life sciences, food and beverages, mission critical/ICT, advanced manufacturing, energy and environmental sectors.

Due to our ongoing success securing large-scale projects we now have a requirement for a CQV Engineer to support us on a project in Leinster.

Who Are We

PM Group is an employee owned, international project delivery firm with a team of 3,700+ people.  We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world’s leading organisations.  We are focused on growing a sustainable business centred around our people, our clients and trade partners.

Responsibilities

• Lead or support the execution of PPQ protocols for drug substance manufacturing systems.
• Develop and manage CQV documentation including:
• Collaborate with cross-functional teams including Engineering, QA, and Manufacturing to ensure alignment on qualification strategy.
• Ensure compliance with GMP, EU/FDA regulations, and internal quality standards.
• Participate in deviation investigations, cycle development, and performance qualification reporting.
• Support vendor FAT/SAT testing and leverage results for qualification.
• Maintain and update the Equipment Validation Master Plan.

Qualifications

• Bachelor’s degree in Engineering, Biotechnology, Pharmaceutical Sciences, or related field.
• Minimum 3–5 years’ experience in CQV within the pharmaceutical or biotech industry.
• Strong understanding of PPQ lifecycle, validation principles, and single-use technologies.
• Experience with electronic validation platforms (e.g., Kneat, ValGenesis).
• Familiarity with automation systems (e.g., DeltaV, PAS-X) is a plus.