Associate Director / Director, Regulatory Affairs CMC

Immunome, Inc. • Bothell, WA

3d • $177,399 - $238,957

About The Position

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.

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.

Requirements

• 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.
• 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.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level