- Fujifilm (Holly Springs, NC)
- …with materials and product movements for manufacturing areas (eg, Drug Substance, Drug Product , Finished Goods and Weigh/Dispense, Raw Material ... of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …to release for use thus sound judgment is essential. The QC Assistant/ Associate Materials Evaluation Coordinator inspects product final container reserve samples ... regions. **Shift: M-F 8am - 4:30pm** The Quality Control Assistant/ Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual,… more
- Pfizer (Sanford, NC)
- …transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation. + Operate within ... loss, and other symptoms. What if there was a way to deliver that cytotoxic drug directly to the cancerous cells and not indiscriminately to healthy cells across the… more
- Pfizer (Sanford, NC)
- …transfers, new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation. + Operate within ... this role, you will: + Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. + Support… more
- Catalent Pharma Solutions (Greenville, NC)
- …fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Quality Compliance Associate is responsible for the ... **Quality Compliance Associate ** **Position Summary** Catalent, Inc. is a leading...Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture,… more
- Fujifilm (Holly Springs, NC)
- …of production systems and to mitigate risks associated with the therapeutic product lifecycle. The Associate Director, CQV collaborates with cross-functional ... of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and… more
- Fujifilm (Holly Springs, NC)
- …team of QA professionals responsible for providing day-to-day risk-based QA support of Drug Substance Manufacturing areas and processes in a fast-paced, dynamic ... **Position Overview** The QA Associate Manager (Operations DSM Upstream) leads and supervises...2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish,… more
- Lilly (Durham, NC)
- …+ Previous experience with combination products, device assembly, pharmaceutical packaging, drug product formulation and filling in aseptic environment. + ... are determined to make life better for people around the world. The Associate Director of Central Engineering / Logistics is responsible for the staffing, training,… more
- Fujifilm (Holly Springs, NC)
- …of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and ... and Maintenance team with the upkeep, troubleshooting, and repair of Good Manufacturing Practice (GMP) equipment. Under the supervision of management or senior… more
- Fujifilm (Holly Springs, NC)
- …of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and ... **Position Overview** The Associate Director, QA for Materials, Supply Chain and...deviations, and changes coming from the QC function. Assures product compliance through Quality systems and effectively ensure initiatives… more