Project Manager, Technical Operations Life-cycle Management

About the role

We're seeking a Project Manager, Life-cycle Management for our Technical Operations team. This role involves supporting the execution of lifecycle management projects within the Tech Ops organization, focusing on commercial products' technical projects such as device changes, combination product post-approval changes, artwork projects, etc.

Responsibilities

• 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.
• 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.
• Contribute to a high-performing, people-centered project management culture that emphasizes clear communication, shared success, and continuous improvement.

Requirements

• You 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 have project management experience in the pharmaceutical, biotech, medical device or consumer health industry.
• You have the ability to lead multiple concurrent cross-functional project teams and drive accountability without direct authority.

Preferred Qualifications

• Nice 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.
• Familiarity with global regulatory submissions (EU MAA, JNDA, US NDA/sNDA) and regional launch planning.

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

Minimal travel expected.

Pay Range

$124,000.00 - $161,000.00 Annual