Visual Inspection Engineer

+2
United Kingdom

+2
United Kingdom

Über

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

United Kingdom

Berufserfahrung

Electronics Engineering
Healthcare

Sprachkenntnisse

English

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