- Grifols Shared Services North America, Inc (Clayton, NC)
- …and accurate data. + Ensures all revalidation requirements are met for equipment, process and cleaning site wide. + Ensures responsible group remains compliant with ... Safety, Performance Development, Quality Stewardship, SOP read and Review, and cGMP training requirements. + Manages validation activities for large scope capital… more
- Lilly (Concord, NC)
- …**Responsibilities:** The QA Materials Disposition Sr. Manager will report to the Associate Director Quality (Materials). The QA Materials Disposition Sr. ... with focus on supporting development of the site e-release process + Manage a team of QA incoming batch...in/supports regulatory inspections, as needed. + Communicates with QA Associate Director Materials and other cross functional… more
- Amgen (Holly Springs, NC)
- …Carolina commercial product release. The Specialist QC Support will report directly to the Director of Quality Control and as a member of this leadership team, you ... **Change Control** + Develop and manage the change control process at ANC in line with FDA, EU GMP,...and 10 years of Quality Control experience OR + Associate 's degree and 8 years of Quality Control experience… more
- Lilly (Durham, NC)
- …ensuring team is trained and training remains in compliance. + Communicates with Associate Director and Quality Representatives on quality issues. + Lead, ... leading and managing a team. + Demonstrated understanding of cGMP regulations related to QA Inspection applications. + Strong...to request an accommodation as part of the application process and any other correspondence will not receive a… more