Associate Director Quality Control

Job Description Global Quality – Large Molecule Analytical Science (GQLMAS) – Quality Control Associate Director, Operational Readiness Job Description At our Wilmington Biotech Campus, we are committed to keeping the patient at the very heart of all that we do and striving to find solutions and treatments for some of the world’s most challenging healthcare needs. The Wilmington Biotech Campus will play a pivotal role in the manufacture of our company’s biologics-based medicines, including the areas of immuno-oncology. This site will establish our company’s internal capability to manufacture high potent compounds when full manufacturing operations begin in 2029. This facility will be a significant supplier of Antibody Drug Conjugates (ADCs) and High Potent Compounds and will also be critical in the future supply of new biotechnology products to it’s global network. Wilmington Biotech Campus – Quality Control Laboratory The QC Laboratory at Wilmington Biotech Campus will be a transformational facility for the analytical commercialization of our company’s pipeline of high potent Biologics. This laboratory will bring together late-stage analytical method development and validation with commercial release testing to deliver significantly improved speed through the analytical lifecycle. The laboratory will be supported by locally based advanced analytical subject matter experts and digital tools to enable an enterprise-wide connected laboratory in support of a new approach to analytical commercialization for high potent Biologics. The laboratory will be operated under our company's Manufacturing Division with close collaboration with Research & Development Division. Reporting to the QC Laboratory Operations Lead, the Quality Control Associate Director – Operational Readiness is accountable for leading the end-to-end QC laboratory operational readiness strategy, integrated planning, and execution in support of the Wilmington Biotech Campus start-up and transition to routine operations. This role provides cross-functional leadership across laboratory operations workstreams, including laboratory start-up, sample management, materials readiness, stability operations, SOPs, training, and inspection readiness. The Associate Director will translate strategic start-up objectives into a single executable readiness plan aligned to the site Integrated Master Schedule, proactively identify risks, drive decisions, and ensure clear governance, escalation, and accountability across stakeholders. The role operates in parallel with construction, commissioning, and qualification activities to ensure the QC laboratory is prepared to accept handover and achieve successful facility approval readiness. Upon transition to steady-state operations, this role will own and continuously improve laboratory operations performance, establish standard work and governance routines, and drive operational excellence across the QC laboratory. Key Accountabilities : Integrated Laboratory Operational Readiness Planning & Schedule Lead the development, maintenance, and governance of the QC laboratory operations readiness schedule across workstreams, ensuring alignment to the site Integrated Master Schedule, critical path, and enterprise readiness milestones. Own cross-functional schedule integration, dependency mapping, and readiness governance to ensure procedures, training, materials, and method-related deliverables are sequenced and executed effectively. Drive schedule convergence and acceleration by identifying dependencies, sequencing conflicts, resourcing gaps, and pull-forward actions; lead escalation of overdue or at-risk deliverables and ensure timely decision-making. Establish laboratory operations readiness stage-gates, define entry and exit criteria, and lead stakeholder reviews to confirm readiness at critical project milestones. Partner with cross-functional stakeholders across Quality, Manufacturing, Supply Chain, Facilities/Engineering, Research & Development Division, IT, and site operational readiness teams to align laboratory operations readiness with site start-up and facility approval timelines. Provide leadership visibility to readiness risks, issues, and decisions through structured governance, dashboards, metrics, and clear communication to site and functional leadership. Additional Laboratory Operational Readiness Activities include; SOPs & Document Readiness Define and lead the document readiness strategy for laboratory operations, including SOPs, Work Instructions, Job Aids, training materials, and operational governance documents required for start-up and routine execution. Ensure document ownership, review, approval, and training timelines are integrated into the master readiness schedule and aligned with facility, equipment, system, and process readiness milestones. Establish document readiness metrics and governance routines to monitor progress, remove barriers, and ensure inspection-ready documentation is available when required. Sample Management Lead the design and implementation of the end-to-end sample management operating model, including receipt, login, storage, tracking, distribution, retention, disposal, chain of custody, and data integrity controls. Partner with Digital, Quality, Research & Development Division, Supply Chain, and laboratory stakeholders to ensure sample workflows, system master data, LIMS functionality, and operational procedures support start-up and routine QC testing requirements. Establish governance and performance measures for sample management to ensure traceability, right-first-time execution, and reliable support of release, stability, qualification, and validation testing. Laboratory Inventory Management Lead the development of the laboratory inventory management strategy for consumables, chemicals, reagents, reference standards, standards, solutions, and supplies required to support QC start-up and sustained operations. Ensure material master data, reorder points, storage requirements, and inventory controls are aligned to start-up sequencing and routine operational demand. Stability Program Operations Provide operational leadership for stability program readiness, including input to facility design, start-up of stability storage and support areas, sample pull scheduling, storage condition management, sample distribution, and supporting procedures. Partner with Quality, Research & Development Division, Manufacturing, Supply Chain, and laboratory stakeholders to ensure stability operations are integrated with site readiness plans, digital systems, and regulatory expectations. Establish operational controls and performance measures to ensure the stability program is inspection-ready and capable of supporting launch and routine commercial operations. Quality & Compliance Ensure all laboratory operations readiness and routine execution activities comply with cGMP, corporate quality policies, data integrity expectations, and applicable regulatory requirements, including FDA, EMA, and ICH expectations. Provide leadership oversight for laboratory operations-related deviations, OOS/OOT assessments, root cause analyses, CAPAs, and change controls; ensure appropriate escalation, impact assessment, and timely closure. Partner with Qual