- University of Southern California (Los Angeles, CA)
- cGMP Quality Control ( QC ) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - ... university's current Good Manufacturing Practices ( cGMP ) facility. The Quality Control ( QC ) Specialist is responsible for designing, developing,… more
- University of Southern California (Los Angeles, CA)
- cGMP Quality Control Lab TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... other highly specialized laboratory tests as appropriate. + Complies with any quality control policies and procedures and maintains required documentation. +… more
- University of Southern California (Los Angeles, CA)
- cGMP Quality Control ( QC ) Specialized Laboratory TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA ... in the university's current Good Manufacturing Practices ( cGMP ) facility. The cGMP Quality Control ( QC ) Specialized Lab Technician is responsible for… 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)
- …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
- Novo Nordisk (Bloomington, IN)
- …Reports to Supervisor. Essential Functions . Independently executes and properly documents cGMP Quality Control testing . Independently operates basic ... and moderately complex cGMP Quality Control equipment ....AND Applies technical understand and functional knowledge to conduct QC laboratory testing as required o Able to perform… more
- Novo Nordisk (Bloomington, IN)
- …Reports to Supervisor. Essential Functions + Independently executes and properly documents cGMP Quality Control testing + Independently operates basic ... and moderately complex cGMP Quality Control equipment +...+ Applies technical understand and functional knowledge to conduct QC laboratory testing as required + Able to perform… more
- University of Southern California (Los Angeles, CA)
- …tech transfer of processes) from cGMP manufacturing and assays to quality control . Develops and reviews standard operating procedures (SOP), protocols and ... implement and execute projects. Provides training support to the manufacturing and quality control teams during tech transfer. + Designs and produces… more
- Catalent Pharma Solutions (Harmans, MD)
- …of experience working in a cGMP QC laboratory. + Experience working in cGMP Quality Control + Experience in cGMP environment and experience with ... The **Scientist, QC ** will oversee the end-to-end contamination control...2 - 4 years of experience working in a cGMP QC laboratory. + Masters' in a… more
- Novo Nordisk (Bloomington, IN)
- …samples from services, water, air, critical systems + Stages materials/components for use within cGMP Quality Control lab + Accurately completes routine and ... to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana… more
- Catalent Pharma Solutions (Harmans, MD)
- …years of relevant experience working in a cGMP environment + Experience working in cGMP Quality Control + Experience with raw material testing and set up ... for patients annually. **The role:** + Lead projects within QC Raw Materials + Authors and Executes Quality... QC Raw Materials + Authors and Executes Quality Records, including Change Controls and Investigations + Sampling… more
- Olon Ricerca Bioscience LLC (OH)
- …education and experience is required. Relevant experience in good laboratory/manufacturing practices (GLP/ cGMP ), laboratory quality control or stability, and ... Job Title: Associate Scientist, QC Essential Responsibilities + Perform HPLC, GC, FTIR,...materials, in-process samples, and finished goods in accordance with cGMP /GLP standard operating procedures + May be able to… more
- Houston Methodist (Houston, TX)
- …work direction of authorized core users working in either production or quality control . + Collaborates with cross-functional teams including research, process ... development, quality assurance and quality control ....daily tasks **GROWTH/INNOVATION ESSENTIAL FUNCTIONS** + Participates with the Quality Assurance Manager and/or cGMP Core Director… more
- Eurofins (Indianapolis, IN)
- …physical sciences field, or at least 3-5 years of laboratory experience in a cGMP pharmaceutical Quality Control laboratory. + Fundamental knowledge of and ... 20 years. The Container Closure Integrity testing laboratory analysts in the Analytical Quality Control Operations (AQCO) organization will serve as a technical… more
- Catalent Pharma Solutions (Chelsea, MA)
- …validation preferred; + Working knowledge of cGMP 's and their application to Quality Control required; + Ability to effectively manage time and prioritize ... ** Quality Control Analyst III** **Position Summary:**...Control Analyst III who is responsible for executing QC testing and related analytical activities supporting product development,… more
- J&J Family of Companies (Raritan, NJ)
- …+ Strong understanding of current Good Manufacturing Practices ( cGMP ) related to the Quality Control ( QC ) laboratory, with the ability to identify gaps ... profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Quality Control **Job… more
- Curia (Albuquerque, NM)
- … regulated industry specific to computer systems validation + Validation experience in a cGMP quality control laboratory or sterile fill finish operations, ... Engineer III is an integral part of the Curia Quality team. This role is responsible for supporting ...Quality team. This role is responsible for supporting Quality Management Systems and Computer System Validation efforts. Additionally,… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …for conducting and implementing activities related to current Good Manufacturing Practice ( cGMP ) site audits, quality control and manufacturing (QCM) ... the following responsibilities: + Conducts thorough review and evaluation of QCM [i.e., quality control and manufacturing] documents and other data received from… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …include managing and conducting activities related to current Good Manufacturing Practice ( cGMP ) site audits, quality control and manufacturing (QCM) ... Manufacturing Practice ( cGMP ) facilities engaged in the manufacturer and/or quality control of dietary supplements and/or pharmaceuticals. * Knowledge of… more
- PCI Pharma Services (Bedford, NH)
- …life science preferred with at least 3-5 years' experience in Pharma or Biotechnology Quality Control cGMP + Alternatively, a BS Degree in Microbiology, ... the future of PCI. Responsible for the day-to-day operations of the QC Microbiology laboratory which include overseeing the environmental monitoring of classified… more