CQV Engineer

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

Posted 3 months ago

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Excellent 4.7

Job summary

The CQV Engineer will lead and execute commissioning, qualification, and validation activities in life sciences manufacturing projects, managing documentation, procedures, and teams to ensure compliance and timely delivery. Requires experience in biotech, aseptic fill/finish, OSD, or gene therapy, and strong communication and problem-solving skills.

Responsibilities

Lead and execute Commissioning, Qualification, and Validation (CQV) activities, managing the documentation lifecycle from SLIA to OQ. Coordinate with vendors and contractors to deliver project deliverables and ensure safety and regulatory compliance.

Qualifications

Commissioning CQV Documentation Process Validation Project Management Regulatory Compliance Risk Management Troubleshooting Validation Vendor Coordination

Requires a BS or MS in a relevant science or engineering field with over 3 years of CQV experience in life sciences. Proficiency in biotech, aseptic fill/finish, or gene therapy manufacturing processes is essential.

English

Benefits

  • Hands On Certifications
  • Professional Training

Company

CAI

CAI

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

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Excellent 4.7
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