About Made Scientific
Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Operating from two U.S.-based manufacturing facilities, Made Scientific combines the agility and entrepreneurial spirit of a specialist CDMO with the global expertise and resources of GC Corporation of South Korea, a global leader in the pharmaceutical and biotechnology sectors.
Position Summary
The Senior Material Handler will oversee Materials Management (MM) operations at our Princeton facility within a GMP-compliant Contract Development and Manufacturing Organization (CDMO). This is a highly autonomous role suited for a professional with extensive experience managing materials in GxP-regulated environments. The ideal candidate will possess deep knowledge of Good Documentation Practices (GDP) and be comfortable making informed decisions in a fast-paced, compliance-driven setting. This position will work closely with cross-functional teams and be expected to operate with minimal supervision while maintaining audit readiness and operational excellence.
Key Responsibilities
- Serve as the primary point of contact and subject matter expert for all materials handling, inventory control, and GMP warehouse operations at the Princeton site.
- Independently receive, inspect, and verify incoming materials, reagents, consumables, and equipment in compliance with GMP standards and company SOPs.
- Forecast material usage to accurately and proactively coordinate with procurement for delivery to meet planned production schedules.
- Execute and document material transactions in ERP or inventory systems, ensuring real-time accuracy and traceability.
- Oversee internal lot assignment, labeling, quarantine, and release workflows, including coordination with Quality Assurance.
- Maintain and monitor storage conditions (ambient, refrigerated, frozen) to ensure compliance with material-specific requirements.
- Accurately stage, issue, and track materials for use in production, quality control, and development activities per BOMs and material request forms.
- Lead cycle counts, discrepancy resolution, and inventory reconciliation initiatives to support audit readiness and operational efficiency.
- Ensure strict GDP-compliant documentation across all materials handling processes and logs.
- Handle hazardous and controlled substances in accordance with internal protocols and applicable safety/regulatory standards.
- Collaborate with QA, Procurement, Manufacturing, and R&D to resolve material issues, ensure readiness of critical items, and maintain status visibility across departments.
- Actively support and initiate deviation reports, nonconformance investigations, and CAPA actions related to material workflows.
- Maintain warehouse organization, drive 5S initiatives, and ensure facility inspection readiness at all times.
- Provide occasional support to the Princeton site, up to 20% of the time, based on business needs.
- Other duties as assigned
Must Haves
- 5+ years of hands-on experience in a GMP/CDMO, pharmaceutical, or biotech environment with increasing levels of responsibility in materials management or warehouse operations.
- Demonstrated ability to operate independently and lead site-level MM functions with minimal oversight.
- Experience with investigating non-conforming materials, out-of-specification test results, and process deviations within a cGMP environment.
- Strong working knowledge of GxP, GDP, and material control requirements under 21 CFR Part 211 or equivalent.
- Experience with material receiving, internal lot tracking, issuance, reconciliation, and compliance documentation.
- Proficiency in ERP or warehouse management systems (SAP, Oracle, NetSuite, etc.).
- High attention to detail and proven ability to execute and troubleshoot material workflows in a regulated environment.
- Physical ability to lift up to 50 lbs and work within temperature-controlled environments.
- Ability to pass a DOT physical examination to drive a company vehicle.
- Excellent communication and cross-functional collaboration skills.
Good to Haves
- Experience in implementing and configuring electronic systems including ERP, MES, LIMS, and QMS
- Proficiency with cold chain logistics, including validated cold storage equipment and shipping practices.
- Familiarity with barcode/RFID-based inventory tracking or warehouse scanning systems.
- Prior experience working in or closely with Quality Assurance or Regulatory Affairs teams, especially regarding material release workflows.
- Understanding of raw material risk classification, vendor qualification processes, and CoA/CofC review procedures.
- Forklift certification and experience operating pallet jacks or other warehouse equipment.
- Basic understanding of temperature/humidity monitoring systems, data loggers, and alert systems.
- Experience leading or supporting warehouse or process audits (internal or external).
- Familiarity with SDS interpretation and hazardous material labeling/handling under OSHA, DOT, or IATA.
Required Degree
- Bachelors degree in logistics, supply chain, or a science-based discipline (e.g., biology, chemistry, biotechnology) required. Associates degree with exceptional experience may be considered.
Physical Requirements
- Ability to perform essential job functions in a warehousing environment, including prolonged periods of sitting or standing.
- Must maintain regular, punctual attendance in accordance with company policies and legal requirements.
- Ability to use a computer and other standard office equipment for extended periods.
- Ability to lift up to 50 lbs.
- Ability to work within temperature-controlled environments.