Senior Manager, Technical Operations Strategy

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 Senior Manager, Technical Operations Strategy on the newly formed Technical Operations Strategy team to help us expand what’s possible for patients with serious diseases. Reporting to the Director, Technical Operations Strategy, you’ll build from the ground up, work across manufacturing, supply chain, and Product Development (CMC Small Molecule, Large Molecule and Gene Therapy) to identify where strategic clarity is needed and go deliver it. What You'll Do: In this role, you’ll have the opportunity to work directly with Technical Operations leadership and functional leaders to define and advance the organization's most pressing strategic priorities. You’ll also: Dig into complex, cross-functional questions, structure them clearly, and bring back a point of view. Identify where the thinking needs to happen and go do it Support manufacturing network decisions by developing scenarios, evaluating trade-offs, and helping leadership understand the long-term implications of site, supplier, and internal versus external manufacturing choices as programs move from clinical to commercial Build and maintain a clear picture of supply risk across the portfolio, identifying vulnerabilities and developing mitigation strategies and continuity plans that protect patient access Contribute to Product Development (CMC Small Molecule, Large Molecule and Gene Therapy) strategy by ensuring that early product development decisions and their downstream implications for manufacturing, supply, and commercial readiness are visible and accounted for in planning Support commercial readiness and launch planning by embedding supply continuity requirements early across the portfolio Build and leverage digital tools and data platforms to develop analytical models, dynamic dashboards, and live data integrations that make supply risk, network planning, and portfolio insights accessible and decision-ready Develop clear, concise materials that help leadership prioritize, escalate, and act across governance and portfolio-level discussions Build relationships at every level, within Technical Operations, across functions including Quality Assurance, Regulatory Affairs, Supply Chain, and Commercial, and with external partners Take on work that does not fit neatly into anyone else's lane and contribute to defining where this group can add the most value Perform other duties and special assignments as needed Who You Are: You have a Bachelor’s degree along with 5 years of experience in roles that required structured thinking, independent problem solving, and clear communication of complex ideas or a Master’s degree and 3 years of experience. You are or you also have: Experience in strategy, business operations, project management, supply chain, or analytical functions within pharmaceutical, biotech, or life sciences Demonstrated ability to take an ambiguous problem, structure it, and deliver a clear recommendation without being told exactly how to get there Strong analytical skills and comfort working with data to build scenarios, assess risk, and support decision-making Excellent written and verbal communication skills. You do not need to be a polished presenter, but you do need to be able to communicate clearly and directly with senior leaders Proven ability to work independently and manage multiple priorities in a fast-moving environment Comfortable operating without a large team or established infrastructure behind you Nice to have (but not required): 7+ years of experience Experience in a strategy consulting, internal strategy, or business operations role, whether at a consulting firm or inside a pharma or biotech company Familiarity with supply chain risk, business continuity, or manufacturing network strategy Exposure to late-stage clinical or commercial launch planning in a regulated environment Experience supporting a portfolio of programs with shared dependencies, including complex modalities such as gene therapy Background in process improvement, operational excellence, or Six Sigma methodologies (Green Belt or Black Belt) PMP or equivalent project management experience Where You’ll Work This is a hybrid role based out of our Bridgewater, NJ office. You’ll have the option to work remotely most of the time, with in-person collaboration when it matters most. Travel Requirements This role requires occasional domestic/international travel (approximately 15-20%). #LI-HYBRID #LI-MC1 Pay Range: $124,000.00-161,000.00 Annual Life at Insmed At Insmed, you’ll find a culture as human as our mission—intentionally designed for the people behind it. You deserve a workplace that reflects the same care you bring to your work each day, with support for how you work, how you grow, and how you show up for patients, your team, and yourself. Highlights of our U.S. offerings include: Comprehensive medical, dental, and vision coverage and mental health support, annual wellbeing reimbursement, and access to our Employee Assistance Program (EAP) Generous paid time off policies, fertility and family-forming benefits, caregiver support, and flexible work schedules with purposeful in-person collaboration 401(k) plan with a competitive company match, annual equity awards, and participatio