This job is with Boston Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. Additional Location(s): US-MA-Marlborough; US-CA-Valencia; US-IN-Spencer; US-MN-Arden Hills; US-MN-Maple Grove 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: This role provides support to the Global Post Market team by leading integrations of companies acquired by Boston Scientific into Boston Scientific’s Post Market system(s) and processes, as well as supporting various projects resulting from regulation changes, business requirements or CAPAs. This role requires strong project management skills, quality system documentation skills, and a proficient understanding of Post Market processes and requirements. Responsibilities may include leading Post Market project teams, identifying key project deliverables, setting appropriate timelines aligning with project milestones, working with cross-divisional/functional representatives to gather required information, communicating project status to senior leadership, and supporting Post Market process improvements and initiatives. Your Responsibilities Will Include: Providing project management, including management of project teams and supporting quality system documentation, for Post Market projects Coordinating parallel tasks and meetings to drive collaboration of multi-site and multi-functional stakeholders to support project deliverables and timelines Leading Post Market workstream for acquisition integration projects Ensuring compliance to US & OUS regulatory requirements Collaborating with Post Market sites and teams Providing audit support (backroom and storyboard preparation) Collaborating with local and international Regulatory and Quality as required Supporting and implementing new SOPs, WIs, and/or KSDs to improve and/or standardize Post Market processes Supporting updates to impacted SOPs/WI Identifying and ensuring training needs are addressed for Post Market requirements Effectively identifying and escalating risks and working to resolve issues Working independently across the organization Participating in the Global Post Market Community In all actions, demonstrating a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Traveling to support projects, as required What We're Looking For In You: Required Qualifications Bachelor’s degree, preferably in a scientific or technical discipline. Minimum of 4 years of medical device industry experience Comprehensive understanding and working knowledge of Trackwise and/or SAS applications Effective research and analytical skills. Competency of Microsoft Office Suite (i.e., Word, Xcel, PowerPoint, Visio, etc.), and Statistical Analysis tools (or equivalent). Working knowledge of FDA, ISO, MDD and the medical device industry quality Strong research, communication, and presentation skills Effective written and oral communication, technical writing, and editing skills Travel approximately LI-DNI