- 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 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and ... maintaining, troubleshooting, and repairing crucial equipment within a pharmaceutical manufacturing setting. Working under the supervision or guidance of experienced… 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 Manager of Instrumentation & Controls (I&C) ensures...designed fit for future operations by utilizing current Good Manufacturing Practice (cGMP) / Good Laboratory Practice (GLP) knowledge,… more
- Pfizer (Sanford, NC)
- …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 ... adverse effects observed with chemotherapy? Pfizer is at the forefront of antibody- drug conjugates (ADCs) biotherapeutic development. ADCs attach a cytotoxic drug… more
- Merck (Wilson, NC)
- …We are seeking a highly motivated individual for the role of Associate Director Engineering - MDCP Technical Lead, supporting the Wilson Packaging Technical ... in a compliant manner are at the core of this position. The Associate Director will routinely face competing priorities, and must manage time effectively, while… more
- Lilly (Durham, NC)
- …who are determined to make life better for people around the world. Associate Director Quality Assurance (QA) Parenteral is responsible for the staffing, training, ... including dispensing, equipment preparation, formulation, filling and visual inspection. The Associate Director will help build a strong quality culture and lead… 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 of Commissioning, Qualification, and Validation (CQV)...leading and executing CQV activities for a large-scale biologics manufacturing facility in compliance with regulatory requirements, including 21… more
- Pfizer (Sanford, NC)
- …this role, you will: + Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. + Support ... new product development, regulatory queries, cost improvement projects, and Drug Product plant support for Cleaning Validation. + Operate...Bachelor's degree with 0 years of experience, OR an Associate 's degree with 4 years of experience OR High… 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
- Grifols Shared Services North America, Inc (Clayton, NC)
- …regions. **Shift: M-F 8am - 4:30pm** The Quality Control Assistant/ Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual, ... materials including, but not limited to, chemicals, labeling components, primary drug container components, process hoses, sterilizing filters, and other critical… more