Recruiter:Spencer Gregory HaleSenior Supplier Quality Engineer.This position could require you to support business that operates on Indian Standard Time (10-14 hour difference from the US time zones).About the role:This Senior Supplier Quality Engineer will be responsible for:Managing a continuous improvement project portfolio focused on simplifying business processes and increasing robustness of quality processes related to sourced finished medical devices in the APAC region.Leading and/or supporting individual, as well as cross-functional, continuous improvement projects.Leading and/or participating in appropriate BSC Communities of Practice to ensure the global processes continuously execute quality outputs at the highest industry/company level.Key responsibilities include:Minimum requirementsEngaging internal and external stakeholders to define and advance continuous improvement opportunities aligned with our Best4 Quality strategy (Best Culture, Best Agility, Best Performance, Best Compliance) and Global Sourcing strategy.Establishing effective communication methods and cadence for reporting project statuses/updates.Championing standards, processes, and best practices across the SQE organization. Serving as a mentor to the SQE community on an as needed basis.Supporting ad hoc requests and special projects, as needed.Demonstrating a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.Travel 10-20% may be required.What we're looking for in you:Minimum requirementsMinimum of a bachelor's degree in engineering with 5+ years related experience in a medical device manufacturing, quality, or regulatory/compliance environmentStrong project management, organizational, and written and verbal communication skillsFlexibility in work hours to accommodate global meetingsContinuous improvement mindset with a passion for Quality Preferred qualifications:Previous experience managing OEM medical device suppliersUnderstanding and practice of the FDA, ISO, and the medical device industry quality requirementsPrior interactions with the following disciplines: manufacturing engineering, post market surveillance, CAPA, risk management, and process engineeringExperience managing individual and cross functional projectsRequisition ID: 577119Among other requirements, Boston Scientific maintains specific prohibited substancetest requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to aprohibited substancetest as a requirement. The goal of theprohibited substancetesting is to increase workplace safety in compliance with the applicable law.
