- Lilly (Durham, NC)
- …will lead investigations and drive implementation of actions associated with deviations . Operations Associate is responsible the daily performance management of the ... a strong safety culture. + Monitor and maintain process team compliance records ( deviations , CAPAs, change controls, etc). + Support Site Leadership to build a… more
- Amgen (Holly Springs, NC)
- …as part of Amgen's plan to be a carbon-neutral company by 2027. ** Specialist - Manufacturing Investigations** **What you will do** Let's do this. Let's change ... part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility...a key member of the team that investigates major deviations in the Amgen North Carolina Biologics Drug Substance… more
- Amgen (Holly Springs, NC)
- …and waste, as part of Amgen's plan to be a carbon-neutral company by 2027. Manufacturing Digital Specialist **What you will do** Let's do this. Let's change the ... your career. Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX batch facility will combine the latest… more
- Fujifilm (Holly Springs, NC)
- **Overview** **Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO** The work we do at FDB has never been more ... and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of… more
- Novo Nordisk (Clayton, NC)
- …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... and oral treatment supply chains. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a...of quality problems in warehouse such as: unscheduled events, deviations , temperature deviations , etc + Resolves/elevates issues… more
- Novo Nordisk (Clayton, NC)
- …of validation documentation + Review & approve complex Change Requests (CR's), Deviations (DVs), CAPAs & other documentation + Perform Self Audits (in conjunction ... of ten (10) years of QA and/or related quality experience in manufacturing , utility and/or packaging systems required, preferably in the pharmaceutical or medical… more
- Novo Nordisk (Clayton, NC)
- …audits & inspections. Review & approval of complex Change Requests (CR's), Deviations (DVs), CAPAs & other documentation. Performs Self Audits (in conjunction with ... Review & approves change control documentation, SOPs & other current good manufacturing practice (cGMP) documentation + Provide coaching to Site regarding quality &… more
- Lilly (Durham, NC)
- …This is an exciting opportunity to help build and operate a state-of-the-art manufacturing site from the ground up. The Health, Safety, Environmental (HSE) ... Specialist will be responsible for the development and technical...+ Experience with CAPA system for HSE changes and deviations + Demonstrated technical leadership skills + Strong communication… more