- University of Southern California (Los Angeles, CA)
- …of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a qualified cGMP Quality Control Associate to join the USC/CHLA cGMP ... of cell and gene therapy products. In addition, the cGMP Quality Control Associate will...reviewing Standard Operating Procedures (SOPs), and ensuring that the Quality Control ( QC ) laboratory remains… more
- University of Southern California (Los Angeles, CA)
- …in the university's current Good Manufacturing Practices ( cGMP ) facility. The Quality Control ( QC ) Specialist is responsible for designing, developing, ... + Supports cGMP manufacturing operations with responsibility for quality control . Performs cGMP batch release testing to ensure pharmaceuticals… more
- University of Southern California (Los Angeles, CA)
- …Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing. Strong attention ... media preparation, cell expansion, harvesting, cryopreservation, and cell culture) and conducts quality control testing to ensure product safety, purity, and… more
- University of Southern California (Los Angeles, CA)
- …years Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing. Strong attention ... USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a qualified cGMP ...control , Corrective and Preventive Actions (CAPA) and change control processes to maintain quality standards. Assists… more
- University of Southern California (Los Angeles, CA)
- …assay development and qualification for product testing. + Lead technology transfer to cGMP manufacturing and quality control , ensuring efficient scaling and ... process and assay development and qualification), support tech transfer of processes to cGMP manufacturing and assays to QC . Develops and reviews SOPs, protocols… more
- Cambrex High Point (Charles City, IA)
- …leadership, and subject-matter expertise for analytical data review activities within a cGMP Quality Control laboratory supporting API and intermediate ... manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career...mentorship to staff on analytical techniques, data analysis, and cGMP practices. + Ensure QC laboratory operations… more
- Actalent (Rockville, MD)
- …+ 2-4 years of relevant experience in a cGMP environment. + Experience in cGMP Quality Control , preferably in a Biologics or CGT setting. + Ability ... Job Title: Quality Control Chemistry Analyst IIJob Description...campaigns. + Support method qualification, validation, and transfer to QC laboratories. + Monitor lab equipment for instrumentation issues… more
- Actalent (Rockville, MD)
- …years of relevant experience working in a cGMP environment. Experience working in cGMP Quality Control , preferably in a Biologics or CGT setting. Solid ... Description Position Summary The Quality Control Analyst II will be...Supports method qualification, method validation and transfer to the QC laboratories, as needed. * Monitors lab equipment for… more
- Actalent (Rockville, MD)
- …in a Life Sciences discipline preferred. + 2 years of relevant experience working in cGMP Quality Control . + Proficiency in Environmental Monitoring of Clean ... Job Title: Quality Control Microbiology Analyst IIJob Description As a Quality Control Microbiology Analyst II, you will play a vital role in supporting… more
- Actalent (Allendale, NJ)
- …discipline. + 3+ years of experience in a cGMP Quality Control Laboratory environment. + Strong knowledge of QC analytical methods and processes. + ... the development and delivery of training programs for our Quality Control ( QC ) team. This...proficient in aseptic cell therapy analytical methods, compliant with cGMP standards, and equipped with the technical expertise needed… more