Boston Scientific
Project Manager II / Fellow, Cardiology
Boston Scientific, Saint Paul, Minnesota, United States, 55112
Project Manager II / Fellow, Cardiology
Work mode: Hybrid Onsite Location(s): Arden Hills, MN, US, 55112 Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing
whatever your ambitions. About the Role
We're looking for a Regulatory or Quality professional ready to take their career to the next level, someone who brings deep process expertise and is excited to step into a leadership role guiding one of Boston Scientific's most critical global initiatives: our ERP transformation. In this role, you'll serve as the key link between our functional teams and technical partners, managing implementation efforts for tools and services that will shape the future of how Boston Scientific operates. You'll gain exposure to senior executives, collaborate with global teams, and establish yourself as a go-to expert in our new enterprise systems. Why This Is an Exciting Opportunity? Be at the center of transformation: Help lead the rollout of a future-ready ERP platform impacting global product development, quality, and compliance operations. Expand your influence: Gain executive visibility and cross-functional experience across PMO, Regulatory, R&D, and Operations. Build new skills: Transition into a project leadership role where your subject matter expertise is your greatest asset. Shape the future: Your voice and experience will influence how Boston Scientific scales globally through technology. Work Mode At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in any of our US Boston Scientific offices at least three days per week. Relocation Assistance Relocation assistance is not available for this position at this time. Visa Sponsorship Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Your Responsibilities Will Include
Partner with cross-functional teams (Quality, Regulatory, R&D, IT) to scope, plan, and execute ERP implementation phases Translate process requirements into actionable project plans Lead risk identification, contingency planning, and issue resolution across a global matrix Collaborate with Software Quality Assurance (SQA) to uphold compliance standards Prepare and present project updates to internal stakeholders and senior leadership Mentor team members on project management best practices Serve as a change champion, building buy-in and enthusiasm across teams, adapting to new systems Required Qualifications
BS/BA Degree in a Scientific, Engineering, or Project Management discipline and/or equivalent experience 7+ years of experience in Regulatory Affairs, Quality Assurance, or a related function in the medical device or healthcare industry 3+ years of experience in cross-functional or program leadership roles Strong understanding of regulated environments (FDA, ISO, EU MDR) and how systems must support them Strategic thinker with the ability to lead through ambiguity and influence at all levels Comfort with process design, change management, and working in global, fast-paced environments A collaborative, systems-oriented mindset and a strong desire to learn and grow as a project leader
Work mode: Hybrid Onsite Location(s): Arden Hills, MN, US, 55112 Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing
whatever your ambitions. About the Role
We're looking for a Regulatory or Quality professional ready to take their career to the next level, someone who brings deep process expertise and is excited to step into a leadership role guiding one of Boston Scientific's most critical global initiatives: our ERP transformation. In this role, you'll serve as the key link between our functional teams and technical partners, managing implementation efforts for tools and services that will shape the future of how Boston Scientific operates. You'll gain exposure to senior executives, collaborate with global teams, and establish yourself as a go-to expert in our new enterprise systems. Why This Is an Exciting Opportunity? Be at the center of transformation: Help lead the rollout of a future-ready ERP platform impacting global product development, quality, and compliance operations. Expand your influence: Gain executive visibility and cross-functional experience across PMO, Regulatory, R&D, and Operations. Build new skills: Transition into a project leadership role where your subject matter expertise is your greatest asset. Shape the future: Your voice and experience will influence how Boston Scientific scales globally through technology. Work Mode At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in any of our US Boston Scientific offices at least three days per week. Relocation Assistance Relocation assistance is not available for this position at this time. Visa Sponsorship Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Your Responsibilities Will Include
Partner with cross-functional teams (Quality, Regulatory, R&D, IT) to scope, plan, and execute ERP implementation phases Translate process requirements into actionable project plans Lead risk identification, contingency planning, and issue resolution across a global matrix Collaborate with Software Quality Assurance (SQA) to uphold compliance standards Prepare and present project updates to internal stakeholders and senior leadership Mentor team members on project management best practices Serve as a change champion, building buy-in and enthusiasm across teams, adapting to new systems Required Qualifications
BS/BA Degree in a Scientific, Engineering, or Project Management discipline and/or equivalent experience 7+ years of experience in Regulatory Affairs, Quality Assurance, or a related function in the medical device or healthcare industry 3+ years of experience in cross-functional or program leadership roles Strong understanding of regulated environments (FDA, ISO, EU MDR) and how systems must support them Strategic thinker with the ability to lead through ambiguity and influence at all levels Comfort with process design, change management, and working in global, fast-paced environments A collaborative, systems-oriented mindset and a strong desire to learn and grow as a project leader