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:3M is establishing two?industry-leading companies, creating value through the spin-off of its Health Care business, while 3M will continue to be a global material science leader, focusing our innovation to win in favorable global megatrends and attractive end markets. This new Health Care Company will be a leading global diversified health technology company with: Proven category leadership Exposure to attractive end-markets Innovation mindset driving improved patient outcomes Collaborative customer relationships Deep global regulatory experience Operational excellence and strong cash flow Strong sales growth and profitability with significant recurring sales We expect the creation of the two companies will be completed by the end of 2023. For now, we will continue to operate as one global company. This role is positioned to drive the success of the "New Health Care Company". 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 RoleAs a Site Quality Manager 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:Standing up new Quality Management Systems (QMS) for a new medical device manufacturing site, and obtaining ISO 13485 certification.Ensuring the suitability and effectiveness of transferred test methods, Device Master Records (DMR), calibration, and other documents and records.Hiring and training the Quality Team.Participating in site Leadership Team ensure the training programs, master validation plan, software qualification and equipment & facility maintenance plans are suitable and effective.Preparing for, managing, and following-up on quality and regulatory audits/inspections conducted by external agencies, notified bodies, customers, and internal functions.Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:Pharmacy degree, with the license active in the Pharmacist Council in BrazilExperience in Regulatory, Quality and/or QMS experience within a heath care regulated industryFluent written and oral communication in both English and PortugueseSupervision or project leadership experienceAdditional qualifications that could help you succeed even further in this role include:Previous experience establishing a new QMSProven ability to lead audit activitiesLean, Six Sigma, and/or Project Manager certificationWork location: Onsite: Sumaré, BrazilTravel: May include up to: 10% domestic and internationalRelocation Assistance: May be authorized
