- Cordis (Irvine, CA)
- …(Non-Conforming Material Reports) and CAPA (Corrective Action, Preventative Action) + Champion cGMP and QSR concepts and procedures + Champion 5S and Lean ... Manufacturing principles + Lead and manage projects (as assigned). Develop resources to accomplish tasks and manage timelines to meet project goals + Develop training programs for new Manufacturing Teammates and coordinate training to revisions/new releases of… more
- Parexel (Sacramento, CA)
- …equipment during audits + Ensure compliance with all regulatory requirements ( cGMP ) and internal policies and procedures **Required Skills and Experience** + ... Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system… more
- University of Southern California (Los Angeles, CA)
- …what it is. USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a dynamic individual to work on the process development ... and gene therapies and other biological products for internal/external users. The cGMP Process Development (PD) Specialized Lab Technician at the USC/CHLA cGMP… more
- University of Southern California (Los Angeles, CA)
- …of internal/external users in the university's current Good Manufacturing Practices ( cGMP ) facility. The Quality Control (QC) Specialist is responsible for ... be responsible for ensuring consistency with current Good Manufacturing Practice ( cGMP ) principles. Job Accountabilities: + Supports cGMP manufacturing… more
- University of Southern California (Los Angeles, CA)
- …staff that make the university what it is. USC's Keck School of Medicine, cGMP Department is seeking a dynamic individual to foster and enhance the translation and ... biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all aspects of operations related to the… more
- Boehringer Ingelheim (Fremont, CA)
- …recognizing and reporting process and equipment anomalies. + Documents work according to cGMP and cGDP. + Adheres to established regulations and follows cGMP ... + Four (4) or more years of experience in cGMP regulated industry. + Ability to concentrate on detail...instructions and document work in a written format applying cGMP standards. + Ability to work as part of… more
- Boehringer Ingelheim (Fremont, CA)
- …implement changes as needed based on assessments. Resolves technical, material and cGMP problems that may impact production deadlines. Provide guidance and help to ... implement changes as needed based on assessments. Resolves technical, material and cGMP problems that may impact production deadlines. Provide guidance and help to… more
- PCI Pharma Services (San Diego, CA)
- …work with the Drug Product team to ensure the successful completion of various cGMP activities. The Associate I will develop a strong understanding of both the ... aspects of the role as well as the quality systems that govern cGMP manufacturing. **Essential Duties and Responsibilities:** To perform this job successfully, an… more
- PCI Pharma Services (San Diego, CA)
- …and standard operating procedures. This position will ensure customer requirements, cGMP requirements, and all foreign and domestic regulations are accurately ... the scope of new projects + Internal Investigations on cGMP issues, trends, and customer complaints + Review and...validation protocols and reports, and executed Batch Records for cGMP compliance and clarity + Process integration and procedural… more
- Kelly Services (Tarzana, CA)
- …cell therapy products by following established processes in full compliance with cGMP . This role also supports manufacturing operational readiness and the successful ... technology transfer of pipeline products using knowledge of cGMP regulations. This is a 3-month contingent assignment, with the possibility of extension based on… more
