Associate Director / Director, Regulatory Affairs CMC

Immunome, Inc.; Bothell (WA); On-site; USD 177,000 - 239,000; Full time

Job summary

Immunome, Inc. seeks an Associate Director / Director, Regulatory Affairs CMC to lead global regulatory CMC strategies across modalities. You will manage key deliverables and ensure alignment with accelerated submission timetables, while communicating with global health authorities.

This role reports to the Senior Director, Regulatory Affairs CMC and partners with Technical Operations, QA, Supply Chain, and Project Management to ensure regulatory compliance and timely filings.

Qualifications

• Bachelor’s degree in a scientific field; advanced degree a plus.
• 7+ years in pharma/biotech with 5+ years in regulatory CMC.
• Hands-on experience preparing CMC submissions for small molecules, biologics, or ADCs.

Responsibilities

• Develop and execute global regulatory CMC strategies for clinical and commercial programs.
• Lead CMC activities on cross-functional teams including ops, QA, supply chain and project management.
• Author and manage CMC sections for INDs, CTAs, IMPD, annual reports and amendments.

Skills

Regulatory CMC knowledge

Cross-functional leadership

Regulatory strategy

Excellent written/verbal communication

Submission management (Veeva RIM)

Education

Bachelor’s degree in a relevant scientific discipline

Advanced degree (MS/PhD) preferred

Tools

Veeva RIM

Job description

Company Overview

Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been submitted to the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-3050, an IND-cleared FAP-targeted radiotherapy; and IM-1617, an IND-cleared solid tumor ADC. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.

Position Overview

Immunome is seeking an Associate Director / Director, Regulatory Affairs CMC, responsible for developing and executing global regulatory CMC strategies across multiple modalities. This individual will manage key deliverables and ensure adherence to accelerated regulatory submission schedules. Reporting into the Senior Director, Regulatory Affairs CMC, the role is responsible for communications and interactions with global regulatory authorities. This person will collaborate cross-functionally with teams including Technical Operations, Quality Assurance, Supply Chain Management, and Project Management to maintain alignment with regulatory CMC strategies and compliance requirements.

Responsibilities

• Develop and execute global regulatory CMC strategies across clinical and commercial stages.
• Serve as the regulatory CMC lead on cross-functional teams, providing strategic input to technical operations, supply chain, quality and project teams.
• Author, review and manage the preparation of high-quality CMC sections for regulatory submission (e.g. IND, CTAs, IMPD, annual reports, pediatric plans, amendments, and marketing applications).
• Lead interactions with global health authorities on CMC topics, including preparation of briefing packages, responses to information requests, and representation at meetings.
• Collaborate with internal and external stakeholders to ensure regulatory compliance and alignment with regulatory CMC strategies.
• Maintain current knowledge of regulations and guidelines (e.g., ICH, FDA, EMA) and keep abreast of changes in the global regulatory environment.
• Support regulatory inspections, as required.

Qualifications

• Bachelor’s degree in a relevant scientific discipline required; advanced degree a plus.
• A minimum of 7 years of relevant pharmaceutical/biotechnology industry experience, including 5+ years in regulatory CMC, or equivalent experience.
• Hands‑on experience with CMC submission preparation for small molecules, biologics, and/or antibody-drug conjugates.
• Experience with regulatory CMC strategy development and health authority interactions.

Knowledge and Skills

• Deep understanding of ICH, FDA and EMA guidelines.
• Outstanding communication, analytical, organizational and time management skills.
• Strong written and verbal communication abilities with attention to detail.
• Ability to effectively lead cross-functional teams.
• Flexible work style with a pragmatic approach to rapidly changing priorities.
• Proficiency in submission management software, such as Veeva RIM.

Washington State Pay Range

$177,399 — $238,957 USD E/E/O

Equal Opportunity Employer

Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

E-Verify

Immunome, Inc. is a participant in E-Verify. Please review the following notices:

E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).