Compensation
$155,000.00 - $155,000.00 / Yearly
Hours Per Week
40
Number Of Positions
1
Job Description
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 Formulation Scientist on the CMC Development team to help us expand what's possible for patients with serious diseases. You'll lead drug product formulation development activities for biologics programs, including high-concentration formulations for mammalian- and bacterial-derived molecules. Additionally, you will provide technical leadership and mentorship to junior scientists, fostering a collaborative and high-performing team environment.
What You'll Do:
In this role, you'll have the opportunity to contribute across early- and late-stage development, supporting formulation design through deep analytical characterization and molecular understanding. You'll also:
Design, develop, and optimize biologics drug product formulations, including aqueous and non-aqueous systems
Develop high-concentration formulations to enable subcutaneous delivery and improved patient convenience
Characterize and optimize excipient systems, buffer conditions, and stabilization strategies as well as evaluate physicochemical stability, aggregation, viscosity, and degradation pathways
Conduct forced degradation and stress studies to understand product stability and define formulation design space
Lead comprehensive analytical characterization of biologic molecules and formulations to inform formulation development as well as characterize higher-order structure, aggregation, particle formation, and colloidal behavior.
Investigate degradation pathways, structure-function relationships, and critical quality attributes and develop, qualify, and implement analytical methods to support formulation screening and optimization
Provide technical leadership for formulation strategy, candidate selection, and developability assessments
Support late-stage activities including comparability, stability strategy, and lifecycle management
Author, review, and approve technical reports, protocols, and regulatory documentation (IND/IMPD/BLA)
Lead and support technology transfer activities to internal manufacturing sites and CDMOs (from a formulation and characterization perspective)
Who You Are:
You have a PhD with 2 years of experience or MS with 6 years of experience in formulation development.
You are or you also have:
Demonstrated experience in biologics drug product formulation development (aqueous and/or non-aqueous systems)
Advanced analytical techniques (e.g., chromatography, spectroscopy, light scattering, calorimetry) to assess structure, stability, and interactions
Strong expertise in analytical characterization techniques for biologics (e.g., SEC, DLS, DSC, spectroscopy methods)
Strong understanding of protein stability, degradation mechanisms, and structure-property relationships
Experience supporting early- and late-stage development programs
Nice to have (but not required):
Degree in Pharmaceutics, Chemistry, Chemical Engineering, Biochemistry, or related discipline
Prior experience mentoring or leading junior scientists or technical staff
Ability to operate effectively in a fast-paced, matrixed environment
Hands-on experience with CDMOs and external development partners
Familiarity with regulatory expectations and filings (IND, IMPD, BLA)
Scientific and technical leadership in drug product formulation and characterization
Strategic thinking across product lifecycle
Quality mindset and regulatory awareness
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 travel (approximately 5%-15%)
Pay Range:
$155,000.00-201,500.00 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 participation in our Employee Stock Purchase Plan (ESPP), and company-paid life and disability insurance
Company Learning Institute providing access to LinkedIn Learning, skill building workshops, leadership programs, mentorship connections, and networking opportunities
Employee resource groups, service and recognition programs, and meaningful opportunities to connect, volunteer, and give back
Eligibility for specific programs may vary and is subject to the terms and conditions of each plan.
Current Insmed Employees: Please apply via the Jobs Hub in Workday.
Insmed Incorporated is an Equal Opportunity employer. We do not discriminate in hiring on the basis of physical or mental disability, protected veteran status, or any other characteristic protected by federal, state, or local law. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. For more information, please refer to our Equal Employment Opportunity and Non-Discrimination Statement on our Careers site.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Unsolicited resumes from agencies should not be forwarded to Insmed. Insmed will not be responsible for any fees arising from the use of resumes through this source. Insmed will only pay a fee to agencies if a formal agreement between Insmed and the agency has been established. The Human Resources department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement.
Insmed is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation to participate in the job application or interview process, please contact us by email at TotalRewards@insmed.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
Applications are accepted for 5 calendar days from the date posted or until the position is filled.
Apply here: https://www.aplitrak.com/?adid=YmJnZW5lcmljLjY4MjI5LjEwNDEyQGluc21lZGNvbXAuYXBsaXRyYWsuY29t
Place of Work
On-site
Requisition ID
R3545-3486