The Sr. Regulatory Affairs Manager will work with a high level of autonomy to oversee the regulatory processes of new product development while managing a regulatory team. This person will lead and contribute to the development of new products and regulatory strategy and conduct assessments of regulatory changes and/or risks throughout the life cycle of the product. Position is located in SLC. It is 95% virtual and candidate is required to go into the SLC office. Essential Job Duties and Responsibilities + Leads team (3 – 4 direct reports) in assessment of regulatory pathways for new and existing products; develops regulatory strategies and plans for submissions to the US and EU. + Communicates potential risks and mitigations associated with regulatory strategies to stakeholders and senior management. + Manages and develops group of regulatory affairs employees carrying out product submission/registration/renewal/change activities. + Delegates, maintains, and updates all necessary lifecycle documentation according to various regulations, including IVDR, and internal procedures. + Directs the preparation and filing of regulatory submissions for US clearance and EU IVDR approval. + Assists in monitoring regulatory developments affecting BMX programs and products and communicates emerging opportunities and concerns to stakeholders. + Directs the regulatory review of labels, labeling, and drives the development of policies to ensure consistency in these reviews. + Develops direct reports regarding required competencies, including, but not limited to, regulatory knowledge and ability to apply this knowledge, effectiveness in team and one-to-one interactions, and verbal and written communications. + Develops functional processes. Ensures functional skills and competencies are reinforced with appropriate tools and templates. + Management of the team and oversees day-to-day responsibilities and workflow. Responsible for interviewing, hiring, and evaluating performance for personnel. + Responsible for timesheet approval, PTO approvals, and attendance tracking. + < 15% Travel required. Minimum Requirements + Bachelor’s degree or equivalent. Science background is preferred. + Masters Preferred. + 6+ years in regulatory affairs or equivalent, medical device/IVD industry, including 4+ years leading projects and directly managing a team and/or multiple employees. Knowledge and Skills + IVD and/or medical device experience required. + 510(k) and IVDR submission experience required (or equivalent). + Very strong written and oral communications skills + Fluent communication in English + Ability to work well within a multicultural environment. + Analyze and understand technical and scientific documents. + Demonstrate initiative and can work both independently and collaboratively in a team structure. + Ability to think strategically, to detect the principle of complex or ambiguous issues, and to put these in the context of larger, systemic issues. + Ability to inspire, motivate, and build the confidence of teams to reach goals, consistently pushing self and others to achieve results. + Proficient with MS Office Suite including Word, Excel, Outlook and PowerPoint + Demonstrate success in supporting both growth and product support projects, including complex projects involving ambiguity, in a rapidly changing regulatory environment.