Associate Director, Quality Control, Biologics

Associate Director, Quality Control, Biologics

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 a highly experienced and strategic Associate Director, Quality Control, Biologics to lead QC strategy and execution in support of our biologics and ADC portfolio. This role will be responsible for oversight of GMP QC activities, including analytical method transfer, qualification and validation, release and stability testing, investigation support, external testing lab management, and QC documentation supporting clinical development and regulatory submissions.

The successful candidate will bring deep technical expertise in biologics and ADC analytical testing, a strong working knowledge of GMP requirements and global regulatory expectations, and the leadership skills necessary to manage cross-functional and external partners. This position offers a highly visible opportunity to build scalable QC processes and ensure Immunome's products are tested with scientific rigor, operational discipline, and patient-centered quality.

• Develop and implement phase-appropriate QC strategies for biologics and ADC programs across drug substance and drug product development, release, and stability.
• Provide scientific, technical, and GMP oversight for QC testing, method lifecycle activities, specifications, reference standards and critical reagent strategies.
• Contribute to the long-term vision for Immunome's QC capabilities, including evaluation of technologies, systems, and external partnerships to support portfolio growth.

• Oversee execution of GMP and non-GMP analytical testing for intermediates, drug substance, drug product, and stability samples in collaboration with CTLs and CDMOs.
• Lead review and interpretation of QC data, trends, OOS/OOT results, deviations, investigations, CAPAs, change controls, and technical reports.
• Serve as the QC representative on cross-functional program teams, ensuring QC deliverables are aligned with CMC timelines.

• Manage external contract testing laboratories and CDMO QC functions to ensure timely, compliant, and high-quality study execution.
• Oversee method transfer, qualification, validation, verification, and troubleshooting activities across external laboratories.
• Establish expectations for documentation quality, sample management, stability pulls, and communication cadence with external partners.

• Author and review QC-related SOPs, protocols, validation and qualification plans, method transfer reports, specifications, CoAs, stability summaries, and regulatory submission content.
• Support preparation of IND, BLA, CTD, and other global regulatory submissions, including responses to health authority questions related to QC and analytical controls.
• Stay informed of emerging regulatory expectations and compendial requirements, integrating relevant guidance into Immunome's QC strategy.

• Lead, mentor, and develop scientists and technical staff, fostering a high-performance culture grounded in quality, accountability, and collaboration.
• Partner closely with Analytical Development, Process Development, Manufacturing, Quality Assurance, Regulatory CMC, Supply Chain, and Program Management to align QC plans with broader development objectives.
• Communicate complex QC data, risks, and recommendations clearly to functional leaders and program teams, enabling timely, science-based decision-making.

• A Bachelor's or advanced degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, or a related field.
• 10+ years of experience in Quality Control, Analytical Development, CMC, or related functions within the biotechnology or biopharmaceutical industry or equivalent; advanced degree may offset some experience.
• Demonstrated experience supporting QC programs for biologics; ADC experience strongly preferred.
• Proven experience with GMP release and stability testing, analytical method transfer, qualification, validation, and lifecycle management.
• Prior experience managing CTLs, CDMOs, CROs, or other external partners supporting regulated testing.
• Experience managing matrixed projects, or external partner relationships in a fast-paced development environment.

• In-depth understanding of GMP standards, data integrity expectations, and global regulatory guidance relevant to biologics QC,…