New · posted Oct 15
Insmed · Biotechnology
Senior Director, Regulatory Affairs CMC - Gene Therapy
- Remote, US
- Remote
- Full-time
- Director
Open until filled
The role
We’re looking for a Senior Director, Regulatory Affairs CMC – Gene Therapy to help us expand what’s possible for patients with serious diseases. Reporting to the VP, Regulatory Affairs Neuro/Other Rare, the Senior Director will serve as the regulatory lead at the CMC sub team level and as an ad hoc member to the Global Program Team (GPT).
In collaboration with the program Regulatory Affairs GPT lead, this individual will define, develop, and implement a well-crafted global regulatory CMC strategy plan to facilitate efficient and competitive product development from early to late-stage development through registration and life cycle management.
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?
Where You’ll Work
This is a fully remote role. It can be performed effectively from anywhere while staying connected to your Insmed team and community. Occasional travel for team meetings or events will be expected.
What you need
Nice to Have (but not required)nice to have
- Advanced degree (Master's, PhD, PharmD) preferred.
- RAC certification desired.
- Knowledge of neurology and/or ophthalmology drug development desired.
- Post approval life cycle management desired.
You must have a Bachelor’s degree in a scientific discipline and 10+ years’ experience in Global CMC Regulatory Affairs and/or relevant product development experience in the pharmaceutical or biotechnology industry. Additionally, you have:
- A minimum of 5+ years of gene therapy orphan (rare) drug development experience.
- A solid understanding of US, EU, and Japanese regulations for biologics, including gene therapy, with the ability to identify the differences in regulations across the regions; strong working knowledge and direct application of relevant ICH quality/CMC guidance, particularly those pertaining to gene therapy product development.
- Experience in the submission and management of the quality aspects of IND/CTA/CTR/IMPDs and global registration applications (e.g., BLA, J-NDA, and MAA), including working knowledge of and experience with electronic submissions (eCTD).
- Experience in leading direct interactions with Health Authorities at key milestone meetings and on complex regulatory matters.
- Demonstrated leadership of global CMC regulatory strategy for gene therapies across early development, registration, and post-approval lifecycle management, ideally for orphan/rare disease programs.
- Experience serving as the Global CMC regulatory lead on a multifunctional, cross-functional development team, with the ability to assess CMC regulatory risk, influence strategic decisions, and exercise sound regulatory judgment on novel or ambiguous issues where precedent or explicit guidance may be limited.
- Experience partnering with Global and Regional Regulatory leads to ensure local regulatory planning and strategy align with and support the overall Global CMC development strategy.
- Strong cross-functional collaboration and communication skills, with the ability to build effective relationships, communicate clearly and concisely, and work successfully in a dynamic, culturally diverse environment.
- Proven ability to manage multiple priorities in a fast-paced, evolving organization, demonstrating strong planning, organization, attention to detail, and follow-through to meet tight deadlines.
- High initiative, flexibility, and sound judgment, with the ability to navigate ambiguity, solve problems independently, and uphold high ethical and compliance standards.
Travel Requirements
This position involves occasional domestic and/or international travel (approximately 10%).
What you'll do
In this role, you’ll have the opportunity to actively participate in cross-functional decision-making discussions to ensure potential regulatory impact on CMC quality development and lifecycle management are communicated and considered. You’ll also:
- Proactively identify and communicate potential CMC risks; define and implement mitigation strategies to prevent or minimize impact to assigned program(s).
- Lead overall CMC regulatory strategy and the preparation of key regulatory dossiers, including meeting requests, briefing documents, INDs, CTA/CTRs, and CTNs, as needed.
- In partnership with the assigned Global Regulatory Lead, Regulatory Operations, and/or third-party service providers, ensure high-quality, compliant, on-time submission activities for initial filings and application maintenance, including IND/CTA/CTR, IMPD updates, and information amendments.
- Provide expert analysis, interpretation, and application of regulatory guidance and requirements from FDA, EMA, PMDA, and ICH, as well as industry and agency best practices and trends, to inform development plans and key stakeholder decisions.
- Monitor the evolving regulatory and competitive landscape to identify opportunities and risks for assigned programs; in partnership with the Regulatory Policy lead, help shape the regulatory environment through comments on draft guidance of direct interest to Insmed.
- Contribute to scientific discussions and collaborations with technical and scientific teams to resolve CMC regulatory issues across development stages and product lifecycles.
- Review regulatory CMC technical documentation prepared by other functions and assess proposed manufacturing, analytical method, raw material, and facility changes for compliance with regional GMP regulations and ICH guidelines.
- Guide and/or lead complex CMC-focused interactions with regulatory authorities and Health Agencies, including FDA, on critical regulatory matters.
- Participate in monthly Global Regulatory Team meetings and serve as the regulatory representative on the specification sub-team; ensure accurate archiving of correspondence and submissions, manage vendor/consultant roles where applicable, and mentor junior regulatory professionals to support continuous learning and operational excellence.
Pay and benefits
$222,000 – $303,000 a year
Employer provided$222,000.00-303,000.00 Annual
Medical, dental, and vision coverage
Generous paid time off
401(k) with company match
Annual equity awards and ESPP
Company-paid life and disability insurance
Learning and development programs
From the posting
About Insmed
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.
Equal opportunity, accessibility and legal noticesInsmed's statements, word for word
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 [email protected] 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.
Important Notice for Job Seekers: Insmed will only communicate with candidates from an @insmed.com email address and will never request payment of any kind during the hiring process. If you'd like guidance on recognizing potential recruitment fraud, please reach out to [email protected].
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 25% above the US median for Regulatory CMC roles at this level.
This roleEmployer provided
Director roles in the US43 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $222,000 | — | $303,000 |
| All US (middle half) | $190,500 | $210,000 | $244,500 |
This role: Insmed's own published range. Comparisons: the base pay employers published on open Regulatory CMC roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory CMC
The general path across 82 open Regulatory CMC roles on Regulatory Jobs, with the titles they carry most. Not Insmed's own promotion track.
Career resources on Regulatory CMC
Skills DNA
What this role leans on
How many of the posting's 31 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership17
- Regulatory submissions7
- GMP and compliance3
- Documentation and SOPs2
- Lab testing and methods1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- FDAFDA IND(official source, opens in a new tab)Investigational New Drug applications
- FDAFDA NDA(official source, opens in a new tab)New Drug Applications
- FDAFDA BLA(official source, opens in a new tab)Biologics License Applications
- FDAeCTD(official source, opens in a new tab)The electronic Common Technical Document format for submissions
Company hiring pulse
Insmed on Regulatory Jobs
- 13
- Open roles
- 13
- Distinct roles
- 3
- Locations
By discipline
- Quality8 62%
- Regulatory4 31%
- Compliance & Safety1 8%
By level
- Director7 54%
- Associate & Specialist3 23%
- Manager2 15%
More roles at Insmed
- View role
Senior Director, Regulatory Affairs CMC
Remote, USDirectorBiotechnology$222K–$303K
- View role
Associate Director, Regulatory Affairs (CMC)
Remote, USDirectorPharmaceuticals$164K–$213K
- View role
Senior Director, Regulatory Affairs - Early Development/Business Development
Remote, USDirectorPharmaceuticals$222K–$303K
- View role
Summer Intern – CMC Quality Assurance, Clinical Programs
Remote, USAssociate & SpecialistPharmaceuticals$42K–$73K
Similar Regulatory CMC roles elsewhere
- View role
Senior Director, Regulatory CMC
Summit TherapeuticsRemote, USDirectorBiotechnology$220K
- View role
Associate Director, Regulatory CMC
Praxis Precision MedicinesRemote, USDirectorBiotechnology$175K
- View role
Senior Manager / Associate Director, Regulatory Affairs CMC (Small Molecules)
Nurix TherapeuticsBrisbane, CADirectorBiotechnology$188K–$209K
- View role
Senior Director, Regulatory CMC
Marea TherapeuticsSouth San Francisco, CA · HybridDirectorBiotechnology$260K–$295K
Senior Director, Regulatory Affairs CMC - Gene Therapy at Insmed
Open until filled. $222K–$303K a year, employer provided.