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Quality Engineers job in Swindon

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Job Ref:  68560195
Employer:  My Job Matcher
Country:  United Kingdom
City:  Swindon
Post Code:  DY3
11/10/2016 16:30
A fantastic opportunity to work for a progressive medical technology company. Our client is among the world's leading suppliers of medical devices and a leading innovator in injection- and infusion-based drug delivery since 1906. Our client offers a warm and friendly working environment and embraces it's employees and their diversities. The role is for a Quality Engineer based in the Swindon area, working within a permanent role offering a very competitive salary and attractive benefits package. A relocation incentive and support could also be available if required, so please contact me for further details. DESCRIPTION To work in project teams responsible for all activities dealing with validation, risk assessment, test methods validation and statistical assessment of NA ensure regulatory requirements are met and that internal procedures are worked to and these activities give added value to the NA a background in statistical analysis (ideally six-sigma green belt), the person will also support plant engineering with Capacity Expansion, Continuous Improvement and Lean projects. They support manufacturing to continually improve Production processes in terms of efficiency, utilisation and waste NA: Responsible for quality related activities within project plans (New Product Introduction, Capacity expansion, Continuous Improvement or Lean projects) are completed fully to agreed timescales and within NA Validation Plans with required change control and validation strategy as part of overall project NA test requirements; coordinate development & validation of test method;Develop sample plans, inspection regimes for product validation and NA analysis of data in process development and validation NA required controls for further process monitoringCreating the required controlled documentation and NA new material introduction within the NA validation protocols and NA out the validation of processes, products and NA out internal and supplier NA to the site audit NA of data for presentation with conclusions and NA communication with other BD sites (i.e. design authority)Supporting plant projects to improve efficiency of production NA scrap levels of production NA the activities required to improve manufacturing NA Quality data and analysis to review meetingsAs product / process expert, support when required Shop-Floor QA for :investigating the reasons for non-conforming product and support the release of blocked stock by QA groupInvestigating and delivering insights to complaints for Complaints Engineer to write the reports within required time scales. QualificationsAdditional information on competencies requiredThe person needs to be self-motivated and able to communicate to Associates at all levels. They need to have a good attention to detail, well organised, methodical in completing documentation and following procedures, able to handle multiple activities concurrently, flexible to suit manufacturing requirements. Some travel to other facilities and customers will be necessary (up to 20% of the time)ESSENTIAL EXPERIENCE At minimum, worked in a quality function with an understanding of quality systemsPrevious Experience of working in a highly regulated industryExperience of working in high volume production environmentThey need to be a competent user of Microsoft packages DESIRABLE EXPERIENCE Medical device industry experience (FDA, ISO 9001, 13485)Ideally has SAP, QDMS and Minitab NA Level Education and six-sigma qualified (green belt/black belt)Knowledge of injection moulding and automated assembly process QUALIFICATIONSHas at minimum an A level standard of education and been trained in statistical techniques (ideally six sigma qualified) and has a knowledge of validation methods. If you have the experience and skill set to match the requirements listed above, enjoy working in a collaborative and engaging culture and are driven by the challenge of assisting in developing innovative solutions for global issues, then we are very interested in speaking with you; so don't delay, please apply using the links NA be advised that due to the expected high volume of applicants we may be unable to reply to everyone individually.
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