CQV Validation Engineer – Pharmaceutical Manufacturing

Company
We are looking for candidates for a site engineering team supporting pharmaceutical technical projects within a regulated GMP environment.

Job Description
This role is for a CQV Commissioning Qualification Validation Engineer (GMP). The engineer will support technical projects with minimal supervision and report to the Senior Manager Validation & Compliance. You will take a hands‑on approach to commissioning and qualification activities, develop and execute test strategies, and drive the creation of system commissioning qualification and validation documentation.

Responsibilities

Develop and update validation documentation, including system‑level criticality assessments, validation and commissioning/qualification plans, risk assessments, test protocols, and requirement traceability matrices

Prepare and maintain commissioning, qualification, and validation summary reports

Lead commissioning, qualification, and validation activities for technical solutions

Provide technical guidance to project teams to ensure implemented solutions follow the validation plan and meet internal customer requirements

Support delivery in line with established site procedures (SOPs)

Carry out additional tasks or projects as requested by your supervisor

Requirements

At least 3 years of experience executing commissioning, qualification, and validation within pharmaceutical manufacturing

Hands‑on commissioning and qualification experience in secondary packaging operations

Experience with secondary packaging systems, including print and inspection systems (e.g., Systech, Cognex)

Experience in Computerized Systems Validation

Strong understanding of how single documents fit into the broader validation picture

Ability to work within internal and/or external reporting relationships

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