Tech Transfer Validation Liaison (CQV Interface)

LSC, Life Science Consultants

Munster

On-site

EUR 65,000 - 95,000

Full time

2 days ago

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Job summary

LSC Life Science Consultants in Ireland (Munster) seeks a Technology Transfer Engineer - Validation Interface to bridge Tech Transfer and CQV/Validation in a GMP setting. Translate transfer requirements into validation protocols and QRAs, coordinating with validation teams to ensure compliant deliverables.

Maintain equipment readiness, track validation dependencies, and escalate scheduling conflicts within the CQV delivery matrix.

Qualifications

Minimum of 3+ years' experience in CQV/validation within a GMP pharmaceutical environment.
Strong knowledge of the site's document hierarchy (Master Plan, QRA, Protocol, Report) or equivalent validation frameworks.
Excellent understanding of EU GMP Annex 1 (2022) and ICH Q9(R1) risk-based qualification principles.
Proven ability to coordinate cross-functional teams and manage validation deliverables effectively.
Strong organizational skills with the ability to escalate and resolve scheduling conflicts promptly.

Responsibilities

Act as the dedicated interface between the Tech Transfer/NPI team and the CQV/Validation function.
Translate transfer requirements into validation protocols and QRAs in collaboration with validation teams.
Coordinate equipment and utility readiness, ensuring prior qualification statuses support product transfers.
Track and report validation dependencies and escalate scheduling conflicts within the CQV delivery matrix.
Support the maintenance of a comprehensive master schedule that integrates transfer and validation activities.