Boston Scientific values: Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance. At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. We’ll help you advance your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.Advancing possibilities for a brighter tomorrow.We are seeking a Quality Engineer P2 on a Defined Term (18 month) basis to join our team.Purpose StatementProvide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products.Key ResponsibilitiesIdentifies and controls Manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and FMEAs.Develops Process Monitoring Systems by identifying critical process steps applying methods to reduce process variation in order to reduce/eliminate the cause of defects.Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development.Assists in creation of Quality Tools & Training Materials by understanding the limitations of existing quality tools and training materials, and by helping to identify more effective tools & materials.Evaluates the adequacy and compliance of systems, operations, and practices against regulation and company documentation. Could serve as auditor of areas of the BSC quality system, such as development and manufacturing, as assigned.Responsible for the final Process Monitor Release for products prior to distribution.Required QualificationsLevel 8 Honours Bachelor Degree in related discipline (STEM)2-5 years’ experience in Manufacturing or QualityExcellent written and verbal communication skillsDemonstrated ability to work with cross functional organizations in a dynamic manufacturing environment to solve problemsStrong command of MS Office – Word, Excel, PowerPointAbility to rapidly learn and use new applicationsPrevious experience in a Quality, or Manufacturing backgroundExperience in the medical device industryWorking knowledge and understanding of FDA, ISO13485, and the medical device industry quality requirements associated with manufacturing and supplier controlsExperience in problem solving and process improvement methodologiesProcess Validation, Risk Management, CAPA experienceBoston Scientific is committed to equal opportunity and affirmative action. Boston Scientific is an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email TalentAcquisitionIre@bsci.com.
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