CQV engineer
Listed on 2026-07-01
-
Engineering
Pharma Engineer, Quality Engineering, Validation Engineer
Job Title
Lead and execute Commissioning, Qualification, and Validation (CQV) tasks with a strong emphasis on safety and compliance.
Deliver C&Q milestones according to established project timelines.
Monitor, track, and report progress of CQV activities to project stakeholders.
Assist in the creation, review, and approval of CQV protocols and procedures in alignment with client requirements.
Provide technical support in the qualification and review of equipment design and related documentation.
Participate in planning for commissioning materials, spares, and consumables.
Optimize allocation of project resources to ensure timely and efficient execution.
Coordinate logistics, support functions, and vendor engagement during the CQV lifecycle.
RequirementsBachelor's degree in Engineering, Chemistry, Life Sciences, or a related field (relevant industry experience may substitute).
Minimum 5 years of CQV or related experience in the Pharmaceutical or Life Sciences sector.
Proven experience working within GMP-regulated environments.
Strong verbal and written communication skills.
Excellent analytical and problem-solving abilities.
Customer-focused mindset with a commitment to quality and delivery.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).