Production Materials Lead

August BioservicesNashville, TN
Onsite

About The Position

The Production Materials Lead is responsible for coordinating, managing, and ensuring the availability and timely staging of materials required for manufacturing operations within a small pharmaceutical CDMO environment. This role serves as a key liaison between Supply Chain, Quality, Warehouse, and Production to ensure timely and compliant material flow aligned with GMP (Good Manufacturing Practices) standards. This position is also responsible for reconciliation of materials that are returned from production and ensuring that they are returned to inventory or discarded per procedure in a timely manner. August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO) headquartered in Nashville, TN. They provide a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, playing a vital role in the global pharmaceutical industry.

Requirements

  • High school diploma/GED or equivalent required.
  • Experience in material coordination, inventory control, or production support
  • Experience with ERP systems (e.g., SAP, Oracle, NetSuite, etc.)
  • Regular and predictable on-site attendance.
  • Strong understanding of cGMP regulations and material control processes
  • Excellent organizational and problem-solving skills
  • Basic computer knowledge
  • Intermediate math skills
  • Ability to manage multiple priorities in a fast-paced, small-company environment
  • Strong communication and cross-functional collaboration skills
  • Detail-oriented with a focus on accuracy and compliance.
  • Ability to follow SOPs, document clearly, and timely.
  • Ability to lift up to 40 pounds at times.

Nice To Haves

  • Bachelor’s Degree preferred.
  • 2-4 years of experience in a pharmaceutical, biotech, or CDMO manufacturing environment or other regulated industry preferred
  • Forklift certification preferred.

Responsibilities

  • Ensure timely availability of raw materials, components, and consumables for production schedules
  • Stage and verify materials (quantities, lot numbers, etc.) for manufacturing batch execution in accordance with batch records
  • Stage inventory for cleanroom materials replenishment
  • Review production schedules and proactively identify material gaps or risks
  • Collaborate with Supply Chain and Planning to align material supply with manufacturing demand.
  • Ensure timely reconciliation of materials returned from production, returning to inventory or discarding promptly.
  • Ensure materials are properly labeled, released, and compliant with GMP requirements
  • Act as primary point of contact for material-related issues on the production floor, minimizing downtime associated with materials issues.
  • Coordinate the receipt of finished goods into inventory post-manufacturing.
  • Inspecting materials for damage, ensuring proper labeling, and managing temperature-sensitive materials (e.g. cold storage or frozen products) with immediate priority.
  • Maintain accurate records for material transactions, ensuring accuracy in both in MRP/ERP systems and all other cGMP documentation
  • Strict adherence to cGMP and Good Documentation Practices, setting the example for good documentation practices and inventory accuracy.
  • Ensure compliance with cGMP, SOPs, and regulatory requirements
  • Support audits and inspections by providing material traceability documentation
  • Using ERP or similar systems, monitor inventory levels and support cycle counts and inventory accuracy initiatives
  • Track material usage and reconcile discrepancies
  • Support inventory optimization to minimize waste and stockouts
  • Work closely with Quality Assurance for material release and deviations
  • Coordinate with Warehouse for material receipt, storage, and issuance
  • Communicate effectively with Manufacturing, QC, and Supply Chain teams
  • Identify and implement process improvements in material handling and flow
  • Support lean manufacturing and operational efficiency initiatives
  • Participate in deviation investigations and CAPA implementation related to materials
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