CQV Engineer – Pharmaceutical Projects

About the role

We are seeking an experienced CQV Engineer to join a fast‑paced project team delivering complex pharmaceutical and life‑science projects. You will support commissioning, qualification and validation activities for GMP‑regulated systems, facilities and equipment, ensuring high‑impact delivery in a technically challenging environment.

Key responsibilities

• Execute CQV activities in line with project schedules and GMP requirements.
• Support commissioning, start‑up and qualification of equipment, utilities and process systems.
• Prepare, review and execute validation documentation, including protocols, reports and traceability matrices.
• Lead or participate in design reviews, FATs, SATs, IQ, OQ and PQ activities.
• Manage qualification documentation throughout the full CQV lifecycle.
• Coordinate with engineering, operations, quality, contractors and vendors.
• Track progress, identify risks and support timely project delivery.
• Assist with change controls, deviations, punch lists and documentation management.

Required profile

• Experience in pharmaceutical, biotechnology, medical device or life‑science industries.
• Strong understanding of GMP and regulated manufacturing environments.
• Proven background in commissioning, qualification, validation or technical operations.
• Ability to work effectively within multidisciplinary project teams.

Required skills

• Commissioning
• Qualification
• Validation
• GMP compliance
• Factory Acceptance Tests (FAT)
• Site Acceptance Tests (SAT)
• Installation Qualification (IQ)
• Operational Qualification (OQ)
• Performance Qualification (PQ)

What we offer

• Opportunity to work on industry‑leading pharmaceutical projects.
• Exposure to cutting‑edge manufacturing technologies.
• Collaborative and supportive team environment.
• Competitive salary or contract rates.
• Potential for long‑term career progression.