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Job Title: Director, Supply Chain and ProcurementJob Description

The Director, Supply Chain and Procurement is a pivotal member of the Operations Leadership Team, tasked with developing and implementing a robust, compliant, and scalable supply chain and procurement strategy. This role supports the clinical to commercial manufacturing, process development, and corporate operations in a 24/7 cGMP environment. The ideal candidate will blend strategic leadership with hands-on execution, possessing extensive experience in cell therapy and thriving in fast-paced, regulated environments.

Responsibilities

+ Develop and execute a forward-looking supply chain and procurement strategy aligned with business growth, clinical timelines, and client program needs.

+ Partner cross-functionally with Manufacturing, Quality, Project Management, and Finance to ensure seamless planning, sourcing, and material readiness.

+ Lead the implementation and optimization of ERP and planning tools to enhance visibility, forecasting accuracy, and cost control.

+ Ensure organizational readiness to support 24/7 manufacturing operations, including availability for off-hours escalations and decision-making.

+ Define and monitor KPIs that drive performance, supply continuity, and continuous improvement across all supply chain functions.

+ Develop and own the end-to-end procurement strategy, including sourcing, contract negotiation, category management, and supplier performance oversight.

+ Establish and enforce procurement governance, workflows, and approval processes to ensure GMP compliance, financial accountability, and traceability.

+ Lead category management for critical spend areas such as GMP raw materials, single-use systems, cold-chain logistics, and contract services.

+ Collaborate with Legal, QA, and Finance to manage the full contract lifecycle, including MSAs, quality agreements, and change control coordination.

+ Identify cost-saving and value optimization opportunities through competitive sourcing, supplier consolidation, and strategic partnerships.

+ Manage relationships with key suppliers, including those providing time-sensitive, GMP-critical, or client-specific materials.

+ Define procurement KPIs and ensure continuous improvement in procurement performance.

+ Oversee two GMP warehouse operations, ensuring compliance with cGMP requirements and readiness for audits or inspections.

+ Maintain validated inventory systems with real-time traceability and oversee materials handling, storage, and dispensing processes.

+ Develop and manage inbound and outbound logistics strategies, ensuring timely, cost-effective, and compliant material movement.

+ Establish contracts with and manage performance of third-party logistics providers.

+ Build, mentor, and lead a high-performing supply chain and procurement team.

+ Foster a culture of accountability, collaboration, and continuous improvement.

+ Set departmental goals, manage budgets, and oversee resource planning.

+ Support employee development through coaching, performance management, and career pathing.

Essential Skills

+ Extensive knowledge in supply chain management and procurement.

+ Strong negotiation skills and end-to-end supply chain knowledge.

+ Experience in the Life Sciences, Pharmaceutical, or Biotech industries, preferably in cell and gene therapy.

+ Experience with ERP implementation.

+ Bachelor’s degree in Supply Chain, Operations Management, Business, Engineering, or a related field; advanced degree preferred.

+ 10+ years of progressive experience in supply chain and procurement leadership roles.

+ At least 5 years in a GMP-regulated CDMO environment across Advanced or Established Modalities.

+ Proven experience in procurement strategy, supplier negotiation, and category management for GMP materials and services.

+ Hands-on leadership experience in warehouse operations and materials management.

+ Strong understanding of GMP compliance, audit readiness, and regulatory documentation requirements.

+ Excellent leadership, communication, and cross-functional collaboration skills.

+ Demonstrated ability to operate effectively in a 24/7 manufacturing environment.

Additional Skills & Qualifications

+ Experience in cell/gene therapy or ATMP environments.

+ Advanced degree in a relevant field is preferred.

Work Environment

This position operates in a 24/7 cGMP environment, requiring readiness for off-hour escalations. The role involves collaboration across various departments, including Manufacturing, Quality, Project Management, and Finance. The work environment is fast-paced and regulated, demanding adherence to GMP compliance and audit readiness. The Director will lead a team and ensure the effective operation of supply chain and procurement functions, including warehouse and logistics management.

Job Type & Location

This is a Permanent position based out of Princeton, New Jersey.

Pay and Benefits

The pay range for this position is $200000.00 - $225000.00/yr.

benefits will be sent to candidates

Workplace Type

This is a fully onsite position in Princeton,NJ.

Application Deadline

This position is anticipated to close on Nov 7, 2025.

About Aston Carter:

Aston Carter provides world-class corporate talent solutions to thousands of clients across the globe. Specialized in accounting, finance, human resources, talent acquisition, procurement, supply chain and select administrative professions, we extend the capabilities of industry-leading companies. We draw on our deep recruiting expertise and expansive network to meet the evolving needs of our clients and talent community with agility and excellence. With offices across the U.S., Canada, Asia Pacific and Europe, Aston Carter serves many of the Fortune 500. We are proud to be a ClearlyRated Best of Staffing® double diamond winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.