CQV Engineer

Overview

Commissioning, qualification and validation of bioprocess equipment and systems.

Key Responsibilities

• commissioning
• iq/oq
• fat/sat
• gmp compliance
• vendor coordination
• cqv documentation

Tasks

-Perform IV, Commission, IQ/OQ and PQ (where applicable) -Collaborate with Vendors and internal stakeholders to ensure timely MC and Turnover -Ensure compliance with GMP, Data Integrity, regulatory requirements -Execute FAT/SAT for Upstream Bioreactors, Harvest Vessels and Downstream Chromatography and UF/DF Skids Looking to speak with experienced CQV Engineers to support Commissioning, Qualification and Validation of Upstream, Downstream, Syringe line and E-beam systems. Projects located throughout Leinster. -Develop and execute CQV documentation

Requirements

• cqv
• 3 years
• gmp
• validation
• electronic validation

What You Bring

Engineers with three years CQV experience highly desirable with a strong understanding of GMP, Validation lifecycle and Electronic Validation.

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About Pm Group

-Founded in 1973, with a mission to deliver high-quality engineering and project management solutions. -A trusted partner for some of the world’s leading companies in sectors like energy, industrial, and pharmaceuticals. -Expertise spans design, construction, commissioning, and project management across diverse industries. -Recognized for delivering complex, large-scale projects across Europe, North America, and Asia. -Notable projects include work in renewable energy, manufacturing, and critical infrastructure. -Continually evolving with a focus on sustainable and innovative solutions to meet future demands.

Sector Specialisms