Associate Director / Director, Supplier Quality and Audits

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 accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets. Position Overview The Director / Associate Director, Supplier Quality and Audits supports the Head of GMP Quality Compliance in building and continuously improving Immunome’s Supplier Quality Compliance and Audit Program. This role leads supplier audit management, vendor governance, compliance monitoring, risk management, quality agreements, CAPA management, and inspection readiness for GxP suppliers and service providers, including CDMOs, CROs, contract laboratories, consultants, and other outsourced partners. It ensures supplier compliance and audit processes are risk-based, inspection-ready, and aligned with regulatory requirements and Immunome’s Quality Management System, while maintaining an effective audit program and governance of outsourced GxP activities. As a virtual biotechnology company, Immunome retains ultimate responsibility for the quality and compliance of outsourced operations, and this role is a key partner in ensuring audit effectiveness, governance, and inspection readiness across the product lifecycle. This role partners closely with Quality Operations, which manages day-to-day supplier oversight, while this position provides independent compliance oversight through risk assessments, audits, governance, and remediation follow-up. Responsibilities Support development and continuous improvement of Immunome’s GxP Supplier Quality and Vendor Management Program. Lead supplier qualification, risk classification, onboarding, and ongoing monitoring of GxP vendors and service providers. Maintain supplier quality records, risk evaluations, audit reports, and performance metrics. Support quality oversight of CDMOs, CROs, labs, consultants, and other outsourced service providers. Partner with stakeholders to clearly define and maintain vendor responsibilities and compliance expectations. Lead negotiation and lifecycle management of quality agreements. Plan and conduct supplier audits and follow-up, including responses, CAPAs, and effectiveness checks. Support inspection readiness for outsourced GxP operations, including regulatory and internal audit preparation. Monitor supplier quality performance, including deviations, CAPAs, complaints, audit findings, and service-level trends. Identify , escalate, and support remediation of supplier quality and compliance risks. Support cross-functional vendor governance meetings and document decisions, actions, and follow-up commitments. Develop and maintain supplier quality procedures, Quality Agreement templates, and related trackers and tools aligned with Immunome’s Quality Management System and regulatory expectations. Support continuous improvement of supplier quality, oversight, audit effectiveness, and inspection readiness. Qualifications Bachelor’s degree in a scientific, technical, or related field; advanced degree preferred. 8+ years of biopharmaceutical industry experience, including direct oversight of third parties performing GxP activities, cGMP manufacturing, testing, or clinical operations , or equivalent experience. Demonstrated experience performing and managing supplier qualification and supplier audit programs. Experience supporting virtual, outsourced, or external manufacturing and service provider models preferred…