Antonio Martinez

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Principal Consultant

Pivotal GxP Supply

May 2026 - Current (3 months)

Sr. Manager, Clinical Supply Chain Operations

Arcus Biosciences

Sep 2021 - Jun 2026 (4 years 10 months)

Strategic leader overseeing end-to-end clinical supply operations to support global Clinical Development Programs. Drive the coordination, procurement, and distribution of investigational drug products, ensuring seamless execution across internal teams and external partners including CROs, suppliers, and clinical sites. Collaborate cross-functionally to define study requirements, develop protocol-specific distribution strategies, and guide vendor selection aligned with project timelines and regulatory standards. Expertly manage bulk inventory, IP shipment schedules, temperature-sensitive logistics (cold chain & CRT), import/export compliance, and IP reconciliation ensuring strict adherence to GMP, GCP, and GDP guidelines. Lead the setup and

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Sr. Manager, Biologics Supply Chain (Department Head)

MD Anderson Cancer Center Therapeutics Discovery Division

Apr 2020 - Oct 2021 (1 year 7 months)

As the department head of Biologics Supply Chain I am responsible for developing, implementing, and maintaining processes to support startup operations for a multi-product (cell and gene therapy, TILs, virus) manufacturing GMP facility. I oversee the site master plan that aligns clinical and commercial supply requirements across the site by overseeing material requirement resources, GMP warehouse operations, logistics, cold chain management, and scheduled supply of manufactured products.

Sr. Manager of Supply Chain (Department Head)

Bellicum Pharmaceuticals Inc

May 2019 - Apr 2020 (1 year)

• Direct and manage supply chain operations as it relates to start-up operations, support of manufacturing operations, clinical operations, commercialization operations, global supply chain, and logistics of GMP materials, equipment, and lab supplies • Direct oversight of Materials Management, Procurement and Logistics departments • Ensure supplier agreements (CDA), Master Service Agreements (MSA), and Scope of Work (SOW) are in place for all critical suppliers and service providers • Manages EU product launch activities such as shipping validation, and commercial product label creation/implementation • Drives continuous improvement of materials movement (ie. pick, pack, kit, stage, ship), storage optimization, and execution of domestic and

Manager, Materials Management

Bellicum Pharmaceuticals Inc

Apr 2017 - May 2019 (2 years 2 months)

• Lead and manage start-up GMP supply chain operations to support multiple cell therapy clinical trials in preparation for regulatory auditing, and commercialization • Manages and supports EU product launch activities such as shipping validation, commercial product label, reagent forecasting, and establishment of supplier agreements • Successfully lead and manage unique demands of cell therapy chain of custody (COC), chain of identity (COI), and risk mitigation of incoming starting materials and outgoing final products • Lead and manage team projects, and business unit growth and development to support multiple clinical trial products • Create, train, and implement standard operating procedures (SOP) and policies • Create process optimizati

Associate Manager, Commercial Accounts

Curia

Jul 2016 - Apr 2017 (10 months)

• Manages the successful manufacture and timely release of multiple client drug products by overseeing the forecasting, scheduling, packaging, labeling, logistics, consignment materials (APIs, Excipients, Reagents) inventories, quotations, contracts (MSA) and customer specific quality agreements • Primary Customer Contact of multiple accounts that effectively leads and assigns work in a dynamic manufacturing setting • Responsible for Product Lifecycle of Forecast through Invoice Proofing, and On Time Delivery (OTD) • Functions as a combination customer advocate, SME, and site liaison between functional departments • Ensure expeditious closure of Problem Reports (PRs) associated with batch release to ensure OTD of final product • Ensures cus

Sr. Supervisor, cGMP Warehouse Operations, and Plant Engineering Maintenance Department (PEM)

AMRI Albany Molecular Research Inc

Jun 2014 - Jul 2016 (2 years 2 months)

• Managed $4 million in raw materials, $3 million in MRO spare parts, and up to $15 million in final product inventory as a multi-departmental supervisor for a 24/7 business operation. • Served as the point of contact and regulatory audit tour lead for regulatory and CMO client GMP warehouse audits. • Implemented and upgraded GMP inventory management systems (ERP, Oracle) conforming to GMP requirements and inventory accuracy for raw materials and MRO product contact spare parts. • Led DEA approval for Schedule II controlled‑substance storage, ensuring facility readiness, security compliance, and effective cross‑functional coordination. • Directed development and revision of GMP‑compliant SOPs for controlled‑substance handling to strengthen

Supervisor, Plant Engineering Maintenance Planning (PEM)

AMRI Albany Molecular Research Inc

Jan 2008 - Jun 2014 (6 years 6 months)

• Supervises, and plans inventory and procurement activities related to the PEM Group operations for a high-volume GMP regulated CMO facility • Supervises multi-shift storeroom technicians and buyers engaged in planning, issuing, and returning MRO spare parts • Responsible for $3 million in engineering, maintenance, and production spare parts • Analyzes production manufacturing conditions to determine needs of product contact, and change parts availability • Leads spare parts replacement of obsolete parts by initiating change control with specifications, blueprints, and schematic • Proactively manages strategic relationships with suppliers for future requirements ensuring 100% quality compliance • Analyze inventory to create proposal for de

Buyer/Planner Plant Engineering Maintenance (PEM)

AMRI Albany Molecular Research Inc

Jan 2005 - Jan 2008 (3 years 1 month)

• Oversees all activities related to procurement of a commodity, from intent to purchase through delivery for an agency regulated GMP manufacturing facility • Designs, and creates procurement reporting systems to gather spending and cost savings of engineering projects • Maintains preventative maintenance work order system in ERP by planning, creating, and updating Preventative Maintenance work orders for facilities, packaging, and manufacturing equipment • Creates and revises Bill of Materials (BOMs) for preventative maintenance work orders to ensure inventory availability • Plans and schedules preventative maintenance work orders for facility shutdowns and manufacturing equipment upgrades • Recruits industry known suppliers that provide h

Equipment Installation, Qualification, and DemoTechnician

intel

Jan 2003 - Jan 2005 (2 years 1 month)

• Responsibilities include supporting site equipment, and facility automation upgrade activities for the world’s largest computer chip manufacturer • Responsible for the installation and removal of production equipment • Prepared factory departmental work summaries to track and establish equipment qualification time lines • Determined project needs for assigned equipment decommissioning and qualification activities • Ensured completion of scheduled electrical, mechanical, and chemical work orders by the contractors • Guided contractors during introduction of equipment into the clean room manufacturing facility to avoid interruption of manufacturing activities

Manufacturing Technician/Operations Coordinator

Intel Corporation

May 1997 - Jan 2003 (5 years 9 months)

• Planner of shift manufacturing operations, production output goals, and quality product results for the Lithography department • Monitored production quality trends during all steps of the manufacturing process (ie. MSC visual inspection, CD and Registration of yield) • Tracked production output to identify indications of work slow-downs or reductions in effectiveness • Established team coverage schedules for the functional area to support output goals • Performed various roles within the team such as Team Lead, Safety Lead, Training Coordinator, and Quality Trending Monitor • Performed everyday technical Lithography area manufacturing operations moving product through all functional area steps down the production line

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