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Kincell Bio

Cell therapy CDMO: development, CMC, manufacturing

Senior Warehouse Supervisor - Supply Chain

Shipping & ReceivingConfirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listed

About the Job

Requirements

  • A high school diploma or equivalent is required; an associate or bachelor's degree in supply chain, logistics, business, or a related field is preferred.
  • At least 6 years of relevant warehouse, inventory control, or logistics experience with a high school diploma; 4 years with a relevant associate's degree; or 3 years with a relevant bachelor's degree. All pathways require at least 3 years in a GMP biotechnology, pharmaceutical, or similarly regulated environment.
  • At least 2 years of experience leading or supervising warehouse personnel, including work assignment, training, and performance coaching.
  • Working knowledge of GMP material controls, inventory status segregation, lot traceability, expiration control, and good documentation practices.
  • Hands-on experience with ERP or warehouse management systems, cycle counting, inventory reconciliation, and Microsoft Office applications.
  • Experience handling temperature-sensitive materials and coordinating cold-chain shipments.
  • Ability to obtain and maintain required powered industrial truck qualifications and role-specific dangerous goods shipping training, where assigned.
  • Ability to prioritize urgent requests without compromising safety or quality.
  • Ability to collaborate effectively with Manufacturing, Quality, Planning, and Procurement in a growing CDMO environment.
  • Frequently stand, walk, sit, use hands to handle materials, reach with hands and arms, and talk or hear.
  • Occasionally climb, balance, stoop, kneel, crouch, or work in refrigerated or frozen storage areas using appropriate protective equipment.
  • Frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds; material handling equipment or team assistance is used for heavier loads.
  • Close vision and the ability to adjust focus for labels, records, and computer screens are required.
  • Must be able to use required PPE and follow site safety procedures when handling materials or operating equipment.

Responsibilities

  • Supervise daily receiving, put-away, picking, staging, issuance, returns, and shipping activities; assign work and adjust priorities to support manufacturing and laboratory schedules.
  • Verify receipt documentation, quantities, lot numbers, expiration dates, labeling, package integrity, and required temperature records; segregate discrepancies and escalate them promptly.
  • Maintain appropriate identification and segregation of quarantined, released, rejected, returned, and expired materials. Issue materials only when their status permits use under approved procedures and Quality authorization.
  • Ensure accurate and timely ERP or warehouse system transactions, including receipts, transfers, issues, returns, and approved adjustments; maintain lot traceability and good documentation practices.
  • Execute cycle counts and physical inventories, investigate discrepancies, and submit reconciliations and proposed adjustments for approval. Apply first-expiry-first-out practices where appropriate.
  • Coordinate material kits, replenishment, and transfers to production areas using approved cleaning, handling, and transfer procedures to prevent contamination and mix-ups.
  • Oversee handling of refrigerated, frozen, and cryogenic materials, as applicable. Verify storage conditions, respond to alarms under approved procedures, and promptly escalate excursions to Quality and the Warehouse Manager.
  • Coordinate time-sensitive shipments with approved carriers and internal stakeholders; verify packaging, shipment records, temperature monitoring, and chain of custody or chain of identity where applicable.
  • Maintain orderly, clean, and inspection-ready warehouse areas; reinforce safe lifting, equipment operation, PPE use, and cold-storage or cryogenic handling practices.
  • Verify that personnel are trained and qualified before performing assigned tasks; provide hands-on coaching and maintain training records with the Warehouse Manager.
  • Document and escalate deviations, damaged goods, shortages, and safety concerns; support investigations, corrective actions, SOP revisions, and change implementation.
  • Track daily workload, inventory accuracy, picking errors, and on-time material delivery; communicate shift handoffs, risks, and improvement opportunities.
  • Support internal, client, and regulatory audits by retrieving records, explaining assigned operations, and completing designated follow-up actions.
  • Direct warehouse associates and material handlers within the assigned area or shift; maintain daily staffing assignments, coverage, and task accountability.
  • Conduct performance reviews for direct reports, set development goals, and provide regular coaching and feedback. Participate in hiring and onboarding with the Warehouse Manager and Human Resources.
  • Monitor training, attendance, and work quality; approve time records and routine time-off requests within delegated authority. Address routine performance issues with the Warehouse Manager and Human Resources, and escalate significant staffing or employee concerns.
  • Promote a collaborative culture focused on safety, quality, reliable delivery, and continuous improvement.
  • Serve as the operational point of contact during assigned shifts and provide coverage for designated Warehouse Manager activities when delegated.
  • Occasional travel for training, other company sites, or logistics provider support may be required.

Desired Qualifications

  • Cell therapy or cryogenic material experience.

About the Company

Kincell Bio

Cell therapy CDMO: development, CMC, manufacturing

Kincell Bio is a CDMO that specializes in cell therapies, offering end-to-end development and manufacturing services for early-stage biotech companies and academic spinouts. It provides analytical development, process development, CMC consulting, and GMP manufacturing to advance autologous and allogeneic CAR-T, CAR-NK, and CAR-M programs from research through clinical trials. Led by experienced CDMO executives and supported by investors, it focuses on early-stage partnerships and has expanded capacity with a new RTP facility to scale mid- to late-stage studies. Its goal is to streamline the path from research to clinical trials and commercial production by delivering scalable, high-quality biomanufacturing and development services for the cell-therapy field.

Company size
51-200
Company stage
Early VC
Total funding
$58M
Headquarters
Gainesville, FL
Founded
2023

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