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At Insmed, every moment and every patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK.For patients, for each other, and for the future of science, we're in. Are you?About the Role:We're looking for a Project Manager, Life-cycle Management on the Technical Operations team to help us expand what's possible for patients with serious diseases. Reporting to the Associate Director, Project Management, you'll to support the execution of lifecycle management projects within the Technical Operations (Tech Ops) organization, with a primary focus on commercial products' technical projects, including device changes, combination product post-approval changes, artwork projects, etc.What You'll Do: In this role, you'll have the opportunity to serve as the central responsible coordinator of activities across cross-functional Chemistry & Manufacturing Controls (CMC) teams to drive project delivery with rigor, transparency, and urgency. You'll also: * Lead end-to-end post-approval project teams internally and with external partners, fostering a collaborative culture that supports team effectiveness, motivation, and accountability. * Collaboratively guide the progression of projects from initial scope creation through lessons-learned post project completion. Develop, maintain, and communicate comprehensive project timelines, key milestones, deliverables, decisions, risks and issues. * Own cross-Insmed communication and follow-ups across all relevant functions to ensure unified execution of project goals. * With the project teams, proactively identify risks and opportunities, develop mitigation strategies with technical experts, and escalate critical issues to ensure timely and informed decision-making. * Serve as a liaison between Insmed project teams and external partners to ensure alignment on project scope, timelines, and deliverables * Represent the PM function in relevant governance forums (e.g., CMC Teams, Tech Ops Project Reviews) and report updates on key milestones, risks, issues, and decisions * Establish and drive structured project frameworks, ensuring clarity of roles, deliverables, and decision-making processes across cross-functional teams. * Champion project management excellence by deploying tools, visuals, and metrics that bring cohesion, visibility, and strategic alignment to the broader Technical Operations organization. * Support the application of project management tools and approaches beyond the PM function, enabling stakeholders across the organization to improve planning and execution. * Support budget and resource planning in collaboration with Technical Operations leadership. * Contribute to a high-performing, people-centered project management culture that emphasizes clear communication, shared success, and continuous improvement.Who You Are:Basic QualificationsYou have a Bachelor's degree along with 5 years of project management experience OR a Master's degree along with 3 years of project management experience.You are or you also have: * Project management experience in the pharmaceutical, biotech, medical device or consumer health industry * Ability to lead multiple concurrent cross-functional project teams and drive accountability without direct authorityPreferred QualificationsNice to have: * Degree in Engineering, Life Sciences, Pharmaceutical Sciences or related field * Understanding of CMC development lifecycle, regulatory submission processes, and post-approval change management * Experience with combination product/medical device post-approval projects * Proficiency with project management tools (e.g., MS Project, Excel, PowerPoint, SharePoint, Smartsheets) * Ability to create clarity and adapt and thrive in fast-paced, regulated environments * PMP certification * Experience supporting commercial launch readiness activities, including packaging validation, and labeling approval workflows * Familiarity with inhaled drug delivery systems and nebulizer-based combination products * Experience with To view the full job description, click hereApply here: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjg3NDM3LjEwNDEyQGluc21lZGNvbXAuYXBsaXRyYWsuY29t