CQV Lead

CAI
Limerick, Munster, Ireland
Full Time
On Site
Senior
0+
Bachelor Degree
Engineering Healthcare Life Sciences

Posted 2 weeks ago

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Excellent 4.7

Job summary

The CQV Lead manages qualification and validation activities for laboratory equipment in a GMP setting, coordinating processes, ensuring compliance, and supporting audits and continuous improvement.

Responsibilities

Lead commissioning, qualification, and validation activities for laboratory equipment within a GMP-regulated environment. Manage the full equipment lifecycle, including documentation, deviations, and continuous improvement initiatives.

Qualifications

Change Control CQV Documentation Equipment Qualification GMP Project Management Qualification Regulatory Compliance Stakeholder Management Validation

Requires a degree in Engineering, Life Sciences, or a related discipline with significant experience in CQV or validation within pharmaceutical or medical device manufacturing. Candidates must possess strong knowledge of GMP requirements and hands-on experience with various laboratory instrumentation.

English

Company

CAI

CAI

linkedin
Pharmaceutical Manufacturing
Location
Limerick, Munster, Ireland
Website
cai.io

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Excellent 4.7
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