Scientist, Analytical Development, Small Molecule

About the role

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?

This role is based out of our Bridgewater, NJ office and requires full-time, in-person presence to support hands-on collaboration, access specialized equipment, and/or operational needs. Travel requirements: minimal travel expected.

Responsibilities

• Take responsibility for small molecule products analytical routine testing (inhalation combination products, tablet formulations, and oral solutions) from early‑stage development through to Phase III and commercialization.
• Ensure all testing is performed in compliance with GMP regulations and internal standard operating procedures (SOPs).
• Accurately record and report test results, maintaining detailed and compliant documentation in accordance with GMP.
• Validate analytical methods using advanced techniques (e.g., HPLC, UPLC, GC, XRPD, Raman, PSD, FTIR, Dissolution and more) to support drug substance and drug product characterization.
• Work closely with formulation scientists, process development teams, and regulatory groups to support CMC activities, ensuring analytical methods meet the necessary regulatory standards.
• Lead pre‑formulation and stability studies for