- Kelly Services (Winston Salem, NC)
- …with incoming material qualification testing and lot release evaluations. + Support process development , validation activities, and data collection for ... **Manufacturing Specialist III - Cell Processing** **Location: Winston Salem...processing techniques, procedures, and regulatory compliance. + Drive continuous process improvement, incident investigations, and deviation resolutions. + Ensure… more
- Biomat USA, Inc. (Research Triangle Park, NC)
- …and quality assurance/control documentation. + Assists in the development of cGMP operating procedures that relate to process , computer systems, and ... out of our RTP, NC Office.** Ensures current Good Manufacturing Practices ( cGMP ) and FDA/Grifols Quality Systems are adhered to throughout the evaluation, review… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The QA Specialist , Drug Substance Manufacturing (DSM) is responsible for partnering in the Quality oversight of DSM project processes. This ... with a focus on consistent policy administration. The QA Specialist , Drug Substance Manufacturing (DSM) ensures QA oversight of...Performs a role within the QA team for the development of documents, processes, and procedures for the DSM… more
- Kelly Services (Greenville, NC)
- **Job Title:** Deviation Specialist (On-Site) **Location:** Greenville, North Carolina **Pay Rate:** $34/hour Contract role **Job Summary:** The Deviation ... Specialist is responsible for the identification, documentation, investigation, and...Lead investigations to determine root causes of deviations and product/ process non-conformances. + Collaborate with cross-functional teams (eg, QA,… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The QA Specialist , Operations is responsible for partnering in the Quality oversight of Drug Substance Manufacturing processes. This role ... their lifecycle, with a focus on consistent policy administration. The QA Specialist , Operations ensures QA oversight of day-to-day activities and resolution or… more
- Catalent Pharma Solutions (Greenville, NC)
- …capacity with potent handling capabilities, ideal for orphan or targeted drug development . The Sample Management Specialist I performs various activities within ... standards, DEA control substances and sample logistics. The Sample Management Specialist I follows all regulatory guidelines, cGMP guidelines, Environmental… more
- Merck (Wilson, NC)
- …writing and deviation investigation + Industrial Electrical, Utility, and HVAC system process improvement and optimization **Preferred** + cGMP in a ... control are needed + Lead in the identification and implementation of process improvement projects, productivity initiatives and corrective actions while focusing on… more
- Merck (Wilson, NC)
- …areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development , Technical Services, Utilities and Validation. ... daily, weekly, and monthly IPT management processes + Lead or support equipment process development and validation activities Compliance + Ensure that assigned… more
- Kelly Services (Wilson, NC)
- **Now Hiring:** Quality Documentation Specialist (Coordinator 2 - Document Control) **Location:** Onsite in Wilson, NC **Duration:** 24-Month Contract (W2) **Pay ... at their Wilson, NC facility. As a Quality Documentation Specialist , you will play a critical role in ensuring...compliance and quality across key documentation systems within a cGMP -regulated environment. This is an exciting opportunity to work… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Quality Systems Specialist Department: Quality Plant Head Location: Monroe, NC START YOUR APPLICATION ... New Biological Entities (NBEs'), with eight molecules in various stages of clinical development . Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US… more