Production Materials Lead

Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing servicesto pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project – including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! 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. Responsibilities Material Coordination & Staging 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. Production Support 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. Documentation & Compliance 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 Inventory Control & Tracking 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 Cross-Functional Collaboration 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 Continuous Improvement 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 Qualifications Education & Experience High school diploma/GED or equivalent required. Bachelor’s Degree preferred. Equivalent combinations of education, training, and relevant work experience may be considered. 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. 2-4 years of experience in a pharmaceutical, biotech, or CDMO manufacturing environment or other regulated industry preferred Knowledge, Skills & Abilities 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. Physical Requirements Light work – exerting up to 40 lbs of force occasionally, and/or up to 10 pounds of force frequently, and/or a negligible amount of force constantly to move objects. Reaching upward and downward, push/pull, stand, Visual Acuity with or without corrective lenses. Climbing stairs/ladders, kneeling/crawling, sitting, stooping/squatting. Finger feeling, handling, push/pull, reaching upward and downwards, standing, walking Must be able to lift up to 40 pounds at times. Forklift certification preferred. EEO Statement August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law. #J-18808-Ljbffr