- Actalent (Sheboygan, WI)
- …the Quality System. The role involves ensuring compliance with internal audits , GMP standards, regulatory and customer requirements, sanitation, pest control, ... Review. Responsibilities + Manage regulatory inspections, customer, and third-party audits by presenting documents and answering auditor's questions. + Schedule… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager . Primary responsibilities for this position will be: perform QC analysis in ... compliance to cGMP in line with standards prescribed by USFDA. Maintain...a ready state of compliance for internal and external audits . + Execute technology transfer of analytical methods for… more
- Sanofi Group (Framingham, MA)
- …the committed scheduled plans + Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, and records ... data, calculations, and information related to his/her tasks, to comply with cGMP and data integrity requirements + Writing/reviewing protocols and reports related… more
- PCI Pharma Services (Madison, WI)
- …the sites' performance and client satisfaction. In conjunction with the General Manager , provides direction as well as develops and implements medium- and long-term ... with all corporate and regulatory requirements** **Responsible for maintaining cGMP compliance and accuracy of all documentation related to manufacturing.**… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager . Primary responsibilities for this position will be: perform QC analysis in ... compliance to cGMP in line with standards prescribed by USFDA. Maintain...a ready state of compliance for internal and external audits . + Execute technology transfer of analytical methods for… more
- Curia (Rensselaer, NY)
- …necessary tools to provide quality metrics, measurements, and reports for internal audits and inspections. Join our talented workforce, where a commitment to ... Development Lifecycle Documents are available for regulatory and client audits , and participate as needed in site audits...date trainings + Other duties as assigned by QA manager and/or QA director Education and Experience: + Bachelor's… more
- Allogene (Newark, CA)
- …documentation, monitoring methods performance and reporting any deviation or discrepancy to manager . This is a daily on-site position in Newark, CA. Responsibilities ... chain of custody * Performs all activities in accordance with cGMP requirements and reports discrepancies. Initiates and completes laboratory discrepancy events… more
- BioLife Plasma Services (Baton Rouge, LA)
- …manufacturing is performed consistently according to current Good Manufacturing Practices ( cGMP ), the Shire Quality System, and other applicable regulations for a ... must also maintain complete and accurate records, in accordance with cGMP . ACCOUNTABILITIES Performs duties associated with Quality (including but not limited… more
- BioLife Plasma Services (Camp Hill, PA)
- …manufacturing is performed consistently according to current Good Manufacturing Practices ( cGMP ), the Shire Quality System, and other applicable regulations for a ... must also maintain complete and accurate records, in accordance with cGMP . **_ACCOUNTABILITIES_** + **Performs duties associated with** **Quality** **(including but… more
- Novo Nordisk (Bloomington, IN)
- …in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include manual, semi-automated and automated inspection, ... in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include solution preparation, master/working cell bank… more
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