Visual Inspection Engineer

Visual Inspections Engineer Team Horizon is seeking a Visual Inspections Engineer for a Visual Inspections Engineer. This person will be responsible for supporting strategy to qualify samples /streamlining processes and taking part in threshold studies. Why you should apply: * This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses. * There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives. * Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally. What you will be doing: * To work as a team member to support Visual Inspection operations in line with all safety, regulatory and organizational requirements. * Develop and modify procedures as needed to support the manufacturing operation. * Participate in process, equipment, and facilities validations efforts and projects implementations. * Review and approve process related commissioning, qualification and validation protocols for completeness and accuracy. * Execute protocols in a timely basis to meet the project schedule requirements. * Participate and lead (as required) Process FMEAs for Visual Inspection * Establish, Lead and Optimize the process for certification of technicians for visual inspection. * Establish and maintain the defect library. * Establish and execute the process for the trending of Visual Inspection Defects * Ensure all Site Visual Inspection procedures are aligned with Global Guidance Documents and Regulatory Requirements * Provide Technical Input to guide the development of SOPs for Visual Inspection. * Leadership of manufacturing and validation activities during project life cycle. * Coordination with internal/external stakeholders for the evaluation of particles/defects * Support of technical transfers for future product introductions to the site. * Investigate process exceptions or malfunction incidents affecting the process. * To liaise with Internal/External Engineering Personnel and Internal/External Quality personnel as required. * Support the Production Team in ensuring that manufacturing process is enabled and maintained to meet the output and yield requirements. What you need to apply: * A relevant third level qualification in an engineering, science or technical discipline (Degree Level or Masters Preferable) * At least three (3) years of total combined experience in Technical/Operations/Operations/Quality or equivalent in a Pharmaceutical and Health Care Organization. * At least three (3) years of experience in the manufacturing environment of a biotechnology, pharmaceutical or health care plant. * Previous experience in manufacturing processes of biotechnological drugs, parenteral drugs, solutions preparation, fill finish, Lyophilisation, sterilisation operations preferable. * Experience in clean utilities is desirable. * Requires a very high level of attention to detail and mental concentration, to ensure accuracy and total compliance with procedures at all times. * Must be results driven striving to meet all targets and metric standards as set by site/department and division leaders. * Understands and supports the principles of Perfect Performance. Requires good knowledge of Company Policies and Procedures and involves working towards general results to achieve organizational needs. * Expected to handle all day-to-day training, learning & development queries, if major problem can refer to Team Manager. Comply with the EHS policy and procedures and demonstrate EHS best practices in all work activities