Senior Director, Analytical Development and Quality Control

The Role:  Generate:Biomedicines is seeking a Senior Director, Analytical Development & Quality Control to set the strategic direction and lead execution of analytical development and quality control for biologics programs in a lean, fully virtual development and manufacturing model. Reporting to the Vice President, Technical Operations, this leader will shape the future analytical and QC operating model for Generate’s biologics portfolio, including analytical strategy, method lifecycle management, release and stability testing, specifications, comparability, external QC operations, GMP readiness, and commercialization preparation across CDMO and contract testing partners. This leader will manage and develop a small senior team, including leaders for Analytical Development and Quality Control, while remaining deeply engaged in critical-path execution. In Generate’s lean model, this means rolling up their sleeves and providing hands-on leadership for high-impact technical decisions, GMP documentation, batch-related analytical data, investigations, deviations, OOS/OOT events, CAPAs, change controls, health authority responses, and inspection readiness. The Senior Director will serve as the senior analytical and QC partner to CMC, Process Development, MS&T, Quality, Regulatory, Supply Chain, and external partners, ensuring protein therapeutics are supported by phase-appropriate, scientifically rigorous, inspection-ready analytical control strategies that advance key company objectives and enable late-stage development and commercialization readiness. Here's how you will contribute: · Define the long-term analytical development and quality control strategy, operating model, governance structure, and external partner network required to support Generate’s biologics portfolio from candidate selection through commercialization readiness. · Lead the development and execution of analytical development and quality control strategies for protein therapeutics from candidate selection through late-stage clinical development and commercialization readiness. · Establish phase-appropriate analytical control strategies, including method development, qualification, validation, specifications, comparability assessments, stability programs, and reference standard management. · Serve as a senior enterprise leader for analytical and QC strategy, consulting with Technical Operations, Quality, Regulatory, CMC, and executive leadership on decisions that affect key company-level objectives. · Build and lead a high-performing analytical organization, directly managing leaders responsible for Analytical Development and Quality Control while fostering a culture of scientific rigor, accountability, collaboration, and quality. · Serve as Generate’s senior analytical and QC representative with CDMOs, contract testing laboratories, and external technical partners, ensuring partner strategies, performance, and issue resolution support program, portfolio, and company priorities. · Provide strategic, technical, and hands-on oversight of CDMOs and contract testing laboratories, ensuring timely delivery of analytical development, GMP release testing, stability testing, and lifecycle management activities. · Serve as the primary analytical and QC representative on cross-functional CMC teams, ensuring alignment of analytical activities with development, manufacturing, regulatory, and clinical supply objectives. · Partner closely with Process Development, MS&T, Quality Assurance, Regulatory Affairs, and Supply Chain teams to ensure analytical strategies support manufacturing readiness, process understanding, product quality, and lifecycle management. · Lead analytical support for technology transfers, process changes, comparability assessments, process characterization studies, and validation readiness activities. · Review and approve critical technical and GMP documentation, including analytical methods, specifications, protocols, reports, method transfer packages, validation documentation, and regulatory submission content. · Provide hands-on leadership during manufacturing campaigns and quality events, including review of batch-related analytical data, investigations, deviations, OOS/OOT results, CAPAs, and change controls. · Lead high-impact technical and GMP issue resolution, personally engaging in critical investigations, deviations, OOS/OOT events, CAPAs, change controls, batch data review, and health authority responses where senior judgment is required. · Drive inspection readiness and ensure analytical and QC activities are executed in accordance with global regulatory expectations, cGMP requirements, data integrity principles, and company quality standards. · Contribute to IND, BLA, IMPD, and other regulatory submissions by developing analytical strategies, reviewing submission content, and supporting health authority interactions and responses. · Establish and monitor key performance indic