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Visual inspection engineer

Galway
Cpl Healthcare
Inspection engineer
Posted: 18 January
Offer description

Visual Inspection Engineer
Summary
The Visual Inspection Engineer supports GMP-compliant visual inspection operations within a pharmaceutical manufacturing environment, ensuring product quality, regulatory compliance, and process robustness. The role provides technical leadership across inspection processes, validation activities, defect management, and continuous improvement initiatives.

Responsibilities

Support visual inspection operations in compliance with safety, regulatory, quality, and organisational requirements

Develop, review, and maintain procedures and SOPs aligned with global standards and regulatory guidance

Participate in and lead process, equipment, and facilities commissioning, qualification, and validation activities

Review, approve, and execute validation and qualification protocols to meet project timelines

Lead and contribute to Visual Inspection Process FMEAs and risk assessments

Establish, lead, and optimise technician certification and training programmes for visual inspection

Develop and maintain the visual inspection defect library and defect trending systems

Provide technical leadership during project lifecycle activities, including new product introductions and technical transfers

Coordinate with internal and external stakeholders on defect evaluation and particle analysis

Investigate process deviations, malfunctions, and inspection-related incidents to ensure robust corrective actions

Support production teams to achieve output, yield, and Right First Time performance

Liaise with Engineering, Quality, Validation, and external service providers as required

Requirements

Degree or Master's qualification in engineering, science, or a related technical discipline

Minimum of three years' experience in a pharmaceutical, biotechnology, or healthcare manufacturing environment

Proven experience supporting operations, quality, or technical functions within GMP-regulated facilities

Knowledge of sterile or parenteral manufacturing processes including fill‑finish, lyophilisation, sterilisation, or solution preparation

Experience with visual inspection processes, validation principles, and defect management preferred

Strong problem‑solving skills with the ability to work under pressure and exercise independent judgement

High attention to detail with a strong commitment to quality, compliance, and Perfect Performance principles

Strong written and verbal communication skills with the ability to influence cross‑functional stakeholders

Demonstrated integrity, ownership, and a results‑driven approach to continuous improvement

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