- Cardinal Health (Seattle, WA)
- …role:_** + Quality Assurance responsibilities include but are not limited to CGMP documentation review related to product release, facilities and equipment, material ... the site manufactures products to meet the requirements of 21 CFR 212 ( CGMP ) + Responsible for the quality of documentation (control, retention, and archival) to… more
- Cardinal Health (Louisville, KY)
- …used for Positron Emission Tomography (PET) scans. **_Responsibilities_** + Handles CGMP documentation review related to product release, facilities and equipment, ... the site manufactures products to meet the requirements of 21 CFR 212 ( CGMP ). + Handles and ensures quality of documentation (control, retention, and archival) to… more
- BeOne Medicines (Pennington, NJ)
- …facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. **Facility Start-Up** : Focused on related activities required to ... execution + Acceptance testing and equipment/automation debugging + Technical training **Hands-On cGMP Operations** : Focused on execution of cGMP manufacturing… more
- Cardinal Health (Phoenix, AZ)
- …improved disease diagnosis, staging, and monitoring. **_Responsibilities_** + Handles CGMP documentation review related to product release, facilities and equipment, ... the site manufactures products to meet the requirements of 21 CFR 212 ( CGMP ) + Handles and ensures quality of documentation (control, retention, and archival) to… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- …raw material manufacturers and distributers. The role supports and maintains all cGMP compliance aspects of Global Procurement operations under the direction and ... may include** + Supports and proactively maintains all Sourcing cGMP procedures, documentation and training related to SOP and...and reports CAPA to support audit closure. + Executes cGMP compliance documents and supports cGMP activities… more
- West Pharmaceutical Services (Kinston, NC)
- …to ensure that product/customer specifications are followed always. Ideal candidates have previous cGMP experience and have the knowledge of how to operate within a ... rooms such as pre-staging, staging, loading, unloading and final packaging, per cGMP standards. + Strict adherence to product/customer specifications. + Ensure that… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …May lead participate on cross-functional teams. Must operate in a highly regulated ( cGMP ) environment and have a strong understanding of cGMP documentation and ... collaboration, respect, professionalism, trust, and integrity. Strong knowledge of cGMP documentation and change control systems including experience with DCM.… more
- Fujifilm (Research Triangle Park, NC)
- …processing steps and activities in a Current Good Manufacturing Practice ( CGMP ) environment. Flexibility with working hours and shift rotation is essential ... right place for you. From our Bioprocess Innovation Center to our cGMP -compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether… more
- Fujifilm (Research Triangle Park, NC)
- …and documents manufacturing processing activities per Current Good Manufacturing Practice ( CGMP ) environment. Flexibility with working hours and shift rotation is ... right place for you. From our Bioprocess Innovation Center to our cGMP -compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether… more
- Bristol Myers Squibb (Summit, NJ)
- …product Value Stream outputs according to Current Good Manufacturing Practices ( cGMP 's) following the current, approved Standard Operating Procedures (SOPs) and Work ... and local laws. + Drive compliance with current Good Manufacturing Procedures ( cGMP ), USP, EU and other global regulatory requirements. + Drive completion, adherence… more