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 DescriptionSoftware Quality Assurance Engineer (New Health Care Company)3M is establishing twoindustry-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 leadershipExposure to attractive end-marketsInnovation mindset driving improved patient outcomesCollaborative customer relationshipsDeep global regulatory experienceOperational excellence and strong cash flowStrong sales growth and profitability with significant recurring salesWe expect the creation of the two companies will be completed by the middle of 2024. 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 Youll Make in this RoleAs a Software Quality Assurance 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:Leads software quality assurance activities throughout medical device software life cycle, including creating software quality assurance plans and cyber risk assessment plans, performing software configuration management and change control activities, facilitating threat modelling and vulnerability assessments, writing reports, performing gap assessments against applicable regulations and industry standards.Implements standard operating procedures for medical device software engineering, takes an active role in continuous improvement of the medical device software engineering process, including authoring, reviewing, and approving procedures, work instructions and templates.Determines software safety classification, software test readiness, software release readiness, cyber risk profile. Is expected to be an active member of the software team during the whole software life cycle, with responsibility for reviewing and approving software requirements, software design, test procedures, test logs, test results, and providing insight to management regarding software project status and software quality metrics.Oversees medical device software development, maintenance, testing, release, safety, and security risk management and ensures compliance with applicable regulatory requirements and industry standards. Immediately elevates to management any major problem with device software that could affect safety, data security, customer usability or system adherence to process requirementsSupports the supplier audit process, internal/external audit process and other processes as applicable, as a subject matter expert in product software providers, and perform other role related duties as assigned by management.Your Skills and ExpertiseTo set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:Bachelors degree or higher (completed and verified prior to start)Three (3) years of experience in medical device software quality or other regulated industry with equivalent software safety and security standards in a private, public, government or military environmentAdditional qualifications that could help you succeed even further in this role include:Working knowledge