?????? ?????????????? ???????????????????????? / ?????????????? ????????????????: ?????????????????? ???????????? ?????? ???????????????????????????????? (?????????????? ?????? ??????????????????; ?????????? ???????????? ?????? ???? ????????????????): * Develop and maintain QA plans and process routings, which reflect intended/actual activities. * Provide support for all quoting activities by participation in initial process design, development, and implementation phases. * Evaluate and support inspection processes via inspection aids and instruction guidelines. * Support all training programs by development and implementation of specialized training sessions for all applicable functions. * Conduct periodic review and maintenance of all documentation files; develop appropriate systems for document storage and access. * Review all supplier or customer discrepancies. Coordinate and track the corrective/preventative action effort. * Provide trend analysis of defects occurring at the customer, supplier and internally. * Participate in the vendor survey activities as applicable. * Drive proactive participation with suppliers and (when possible) aid in their process improvement efforts. * Interface with all departments as applied to the Policies and Procedures with special regard to ISO, EN4600 and GMP documentation. * Monitor departmental activities and provide technical and logistical guidance/support for the quality engineering staff as applicable. * Interface and provide technical support on quality issues with the customer as needed. * Support and focus corrective action efforts and utilizing the SPC data and corrective action tracking package and create and implement any meetings, procedures, or team-building concepts as necessary as part of the corrective/preventative effort. * Serve as liaison between the company and suppliers or customers on quality related issues. * Improve technical support for the quality organization. * Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor. * Comply and follow all procedures within the company security policy. ?????????????? ????????????????????????: * Bachelor's degree required * 2 years related experience; or equivalent combination of education and experience in Medical Device and/or Pharma Industry. * Preferably with Knowledge/experience of manufacturing engineering, exposure to high volume medical device or pharma automated assembly lines. ????????????/????????????????????: * Excellent organization, communication, computer & presentation skills. * Excellent initiative, decision making and be able to work in a core team environment. * Excellent time management skills. * Solution driven with emphasis on performance and results. Adecco Ireland is acting as an Employment Agency in relation to this vacancy. Skills: Pharmaceutical Quality Manufacturing
