Quality Assurance Manager

*** Sponsorship not provided | must be eligible to work in the UK ***

Develops, implements and maintains the activities of quality control systems. Oversees development and implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products. Develops budget and monitors expenditures.
Ensures all aspects of ISO
13485
, relevant standards and applicable regulatory requirements are met and upheld within the QMS and the Organisation.

Makes recommendations for corrective action necessary to ensure conformity with quality specifications. Ensures finished products conform to government and company standards and satisfy good manufacturing practices regulations. Selects, develops and evaluates personnel to ensure the efficient operation of the function. First level of managerial position. Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals.

Works on issues of a diverse scope where analysis of situation or data requires evaluation of a variety of factors. Typically manages a department of Professional track employees but may also have support track direct or indirect reports.

• Ownership & management of customer complaints investigations (CAPA) with focus on preventive actions implementation and their effectiveness verification; preparation, analysis & distribution of associated KPI metrics
• Active participation in continuous improvement and maintenance of company’s integrated QEHSMS accredited to ISO
  13485/9001/14001/45001 with the emphasis on medical devices manufacturing compliance – development, review & update of relevant QEHSMS documentation; internal audits etc.
• Active participation in suppliers quality management – review & approval process ; supplier audits ; purchased product control plans preparation, review and approval
• Risk management oversight: preparation of process FMEAs, manufacturing process verification & validation management
• Participation in Optical Measuring System programming for inspections of purchased product (training provision to be given)
• Quality Engineering support as part of day‑to‑day business as well as part of the cross‑functional teams for continuous improvement activities
• Any other duties and responsibilities as required

• Working Knowledge of ISO
  13485/9001/14001/45001 with the emphasis on medical devices manufacturing compliance – development
• Workplace Health and Safety Legislation