SummaryThe 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.ResponsibilitiesSupport visual inspection operations in compliance with safety, regulatory, quality, and organisational requirementsDevelop, review, and maintain procedures and SOPs aligned with global standards and regulatory guidanceParticipate in and lead process, equipment, and facilities commissioning, qualification, and validation activitiesReview, approve, and execute validation and qualification protocols to meet project timelinesLead and contribute to Visual Inspection Process FMEAs and risk assessmentsEstablish, lead, and optimise technician certification and training programmes for visual inspectionDevelop and maintain the visual inspection defect library and defect trending systemsProvide technical leadership during project lifecycle activities, including new product introductions and technical transfersCoordinate with internal and external stakeholders on defect evaluation and particle analysisInvestigate process deviations, malfunctions, and inspection-related incidents to ensure robust corrective actionsSupport production teams to achieve output, yield, and Right First Time performanceLiaise with Engineering, Quality, Validation, and external service providers as requiredRequirementsDegree or Master's qualification in engineering, science, or a related technical disciplineMinimum of three years' experience in a pharmaceutical, biotechnology, or healthcare manufacturing environmentProven experience supporting operations, quality, or technical functions within GMP-regulated facilitiesKnowledge of sterile or parenteral manufacturing processes including fill-finish, lyophilisation, sterilisation, or solution preparationExperience with visual inspection processes, validation principles, and defect management preferredStrong problem-solving skills with the ability to work under pressure and exercise independent judgementHigh attention to detail with a strong commitment to quality, compliance, and Perfect Performance principlesStrong written and verbal communication skills with the ability to influence cross-functional stakeholdersDemonstrated integrity, ownership, and a results-driven approach to continuous improvement