Campus Pride Jobs

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here continue to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions.As it was with 3M, at Solventum all q ualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.Job Description:Program Project Manager3M 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 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 end of the first quarter of 2024. We will continue to operate as one global company. This role is positioned to drive the success of the "New Health Care Company".The Impact You'll Make in this RoleAs a Project Manager of the Strategic Materials Supply Continuity Program, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world.Our projects are at the forefront of medical device technology, focusing particularly on the use and integration of adhesives, chemicals and materials. Your role will be pivotal in steering these projects towards success, making a significant impact in the medical field. Previous experience in medical devices, particularly with adhesives and chemicals, is highly regarded.Here, you will make an impact by:Assisting the Program VP in developing and implementing strategies specific to the supply continuity program upon the separation from 3M. Project management specific projects in exploration and evaluation of alternative or/and new technologies that can secure supply independence.Leads cross-functional teams to deliver project milestones on time, within budget, and in alignment with the strategic objectives of the program. This includes effective management of project scope, resources, value proposition, technical approaches, manufacturing options, stakeholder communication ultimately leading to successful realization of the program solution(s).Implements project management best practices to ensure the smooth execution and completion of projects. This involves establishing clear project plans, risk management strategies, and quality control measures to meet the high standards required in the medical device or regulated industry.Determines project requirements and objectives by conducting detailed needs analyses, feasibility studies, and consultations with internal stakeholders and external partners. This role requires a keen ability to collaborate with the technical team to translate complex material and chemical specifications and performance requirements into actionable project plans.Willingness to be on-call as needed to address critical project issues or emergencies. This position requires a high level of dedication and flexibility, acknowledging that timely responses can be crucial to project success and continuity of supply.Your Skills and ExpertiseTo set you up for success i this role from day one, 3M requires (at a minimum) the following qualifications:Bachelor's degree or higher in an Engineering or Science discipline from an accredited University AND minimum of 7 years of in the healthcare/chemical industry a private, public or governmental environmentIn addition to the above requirements, the following are also required:Minimum of 3 years of project management and/or team leadershipMinimum 5 years of experience with medical devices and FDA/ISO requirements.Additional qualifications that could help you succeed even further in this role include:Project Management Institute's Project Management Professional (PMP) certificationExcellent communication skills (oral, written and presentation)Ability to influence including clarifying risks and opportunities with stakeholders.Experience leading global cross-functional teams.Microsoft Office and Project proficientExperience with New Product Introduction Process and Executing Gate Reviews, or other Phase-Gate ProcessNew product development or product life cycle maintenance such as product engineering experience a plusExperience in chemicals, polymers and adhesives, and in manufacturing transfer to external manufacturing is a plus.For current employees, internal transfer restrictions may not apply. For more details, contact your local recruiter/HR team.Work location: Maplewood, MN/ San Antonio TX (Hybrid Eligible with home base in Maplewood, MN)Travel: May include up to 15%Relocation Assistance: May be authorizedMust be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).Supporting...Equal Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity