Senior Manager, Technical Operations Strategy
Insmed Incorporated
Summary
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.
Job description
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%).
Requirements
- Bachelor's degree with 5 years of experience in roles requiring structured thinking, independent problem solving, and clear communication of complex ideas, or Master's degree with 3 years of experience
- 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
- 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
Benefits
- Medical, Dental & Vision
- Mental Health Support
- Wellbeing Reimbursement
- Employee Assistance Program
- Paid Time Off
- Fertility & Family Benefits
- Caregiver Support
- Flexible Work Schedules
- 401(k) Matching
- Annual Equity Awards
- Employee Stock Purchase Plan
- Life & Disability Insurance
- LinkedIn Learning
- Skill Building Workshops
- Leadership Programs
- Mentorship Connections
Company overview
Insmed Incorporated is a people-first global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases. Headquartered in Bridgewater, New Jersey, with offices and research locations throughout the United States, Europe, and Japan, the company focuses on delivering first- and best-in-class therapies for underserved patient communities. Insmed's portfolio includes two approved therapies for chronic lung diseases: ARIKAYCE for Mycobacterium avium complex lung disease and BRINSUPRI for non-cystic fibrosis bronchiectasis. The company is advancing a diverse pipeline of mid- to late-stage investigational medicines and cutting-edge drug discovery programs spanning gene therapy, AI-driven protein engineering, RNA end-joining, and synthetic rescue technologies. Recognized as the No. 1 Science Top Employer for five consecutive years, Insmed employs 1,001-5,000 professionals globally and maintains a strong commitment to innovation, patient-centricity, and corporate responsibility.