3M has a long-standing reputation as a company committed to innovation. We provide the freedom to explore and encourage curiosity and creativity. We gain new insight from diverse thinking, and take risks on new ideas. Here, you can apply your talent in bold ways that matter. Job Description: Job SummaryWe are currently seeking a highly skilled and experienced individual to join our team as a Senior Quality Engineer. In this role, the successful candidate will play a crucial role in ensuring product quality assurance support for Medical Products and management of quality system to meet Korea FDA requirements The ideal candidate for this position will have a strong background in quality engineering within the Medical Products with a deep understanding of ISO 13485 requirements, Korean Medical Device, Quasi-drug, and Cosmetic regulations. They should possess excellent communication and leadership skills, with the ability to collaborate effectively with cross-functional teams. Strong analytical and problem-solving abilities, along with a commitment to continuous improvement, are also essential. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact You’ll Make in this Role As a Senior Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Working closely with manufacturing, laboratory, and regulatory functional leaders locally and globally, to drive standardization for processes and records related Medical Products. This includes ensuring that all QMS related activities are followed and consistently implemented to ensure compliance with Korea FDA requirements. Key responsibilities of the Senior Quality Engineer will include: + Enhancing Customer Satisfaction – Implement quality activities aligned with division quality strategy to enhance customer satisfaction. + Quality System Leadership – Establish and maintain the quality management system in Korea for Medical Device, Quasi-drug, and Cosmetics. + Leading Quality Qualification in New Product and Product Change Projects - Ensure new or modified products to meet customer, regulatory, marketing requirements. + Resolving Quality Issue – Lead the communication between lab and plant to minimize the lead time to resolve the issue and complaint sample analysis. + Supplier Product Quality Management – Establish supplier product quality plans to ensure the outsourced product to meet its requirements. + Product quality – Support product quality such as design issue follow-up, sampling plan revisit for product release, document revision, etc. Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: + Bachelor’s degree or higher in an engineering or science discipline (completed and verified prior to start) from an accredited institution + Three years of combined experience in a Manufacturing, Production, Quality and/or Laboratory role in a private, public, government or military environment + 5 years of Experience in Medical Device industry Additional qualifications that could help you succeed even further in this role include: + Bachelor’s degree or higher in a Science, Technology, Engineering or Mathematics (STEM) or related discipline from an accredited university + Experience in Medical Device QMS – ISO 13485, MSAP, MDD, Korean FDA regulations + Certifications in quality engineering, quality auditing or quality management according EOQ standard or comparable + Microsoft Office proficient ​ ​ Condition + Type: 정규직 (수습기간 3개월) + Location: 한국3M 동탄 기술연구소 ( 경기 화성시 삼성1로5길 7 ) Application Guidelines (입사 지원 시 주의사항) + Click ‘Apply ’ button + Fill in basic information such as employment ?and education + Upload your both of Korean/English Resume (merge your files into one file )(이력서 내 경력기술서 및 자기소개서 포함) Others + 해외여행에 결격사유가 없어야 합니다. + 국가유공자 및 보훈대상자(veteran) 은 관련 법규에 따라 우대 합니다. 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