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Principal Supplier Quality Engineer | Quality Engineer in Quality Assurance Job in Maple Grove MN 1

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Principal Supplier Quality Engineer

Location:
Maple Grove, MN
Description:

Recruiter: Spencer Gregory Hale Principal Supplier Quality Engineer About the role: The Sourced Finished Medical Device (SFMD) organization at Boston Scientific is a global, passionate team that oversees a diverse network of suppliers which manufacture finished devices for BSC distribution. The Principal Supplier Quality Engineer will demonstrate a primary commitment to patient safety and collaborate with cross:functional internal/external resources to continually improve our supplier's manufacturing processes. This is a hybrid role with the expectation to be in the office 2 daysa week. This position will be located in Maple Grove, MN. Your responsibilities include: Sustaining Engineering: : Evaluates and communicates quality issues to suppliers and applies sound, systematic problem:solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation.: Proactively assesses supplier capabilities through direct on:site visits and technical discussions. Coordinates the evaluation of proposed changes at suppliers.: Plans and leads audits of suppliers to assess compliance with regulatory and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow:up, and confirmation of follow:up actions. New Product Development: : Lead the execution of SFMD quality deliverables and collaborate with cross:functional new product development teams to onboard finished medical device suppliers.: Generate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations. Quality System Champion: : Collaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents.: Identifies and advises management on potential improvements to quality systems and processes in the company.: Champions 100 compliance to company policies and SOP's. Minimum qualifications: : BS degree in engineering or technical field with 9 years or MS degree and 7 years relevant experience.: Experience in the medical device, automotive, aeronautical, semiconductor, or other regulated industry.: Project management: the ability to influence cross:functional global teams spanning quality, operations, R and D, and sourcing.: Experienced in Problem Solving methodologies; including the ability to lead multifaceted investigations across complex supply chains.: Experience in process validation, design controls, risk management, and CAPA.: Ability to rapidly learn and use new software applications (e.g., PLM, ERP).: Domestic and international travel up to 25. Preferred qualifications: : Ability to work independently; organized and self:driven. : Articulate communicator adept at packaging and appropriately scaling information to the intended audience.: 7+ years of medical device engineering experience.: Experience with catheter design and/or manufacturing.: Previous support for high volume manufacturing. : Leadership experience on a materials or service commodity team.: Lead auditor of quality systems experience (ISO 13485 or similar).: ASQ certification (CQE, CBA, SSGB, SSBB) strongly desired.: Fluent in Spanish Requisition ID:579500 Among other requirements, Boston Scientific maintains specificprohibited substance test requirements for safety:sensitive positions. This role is deemed safety:sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicabl
Posted:
April 7 on Tip Top Job
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