- University of Southern California (Los Angeles, CA)
- cGMP Quality Control (QC)...GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work ... internal/external users in the university's current Good Manufacturing Practices ( cGMP ) facility. The Quality Control ...current Good Manufacturing Practices ( cGMP ) facility. The Quality Control (QC) Specialist is responsible for… 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 ... laboratory tests as appropriate. + Complies with any quality control policies and procedures and maintains... laboratory experience, knowledgeable in use of specialized laboratory equipment. Working knowledge of lab procedures,… more
- University of Southern California (Los Angeles, CA)
- cGMP Quality Control (QC) Specialized Laboratory...Practices ( cGMP ) facility. The cGMP Quality Control (QC) Specialized Lab ... TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - Quality - Control --QC--Specialized- Laboratory -Technician\_REQ20159957/apply) Keck School of Medicine Los Angeles, California… 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 to ... cell therapy and cGMP manufacturing. + Prepares, calibrates, and maintains laboratory equipment for use. Participates in routine lab maintenance and ensures… 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 ... and process development reports. Authoring CMC documentation. + Oversee lab setup and work with cGMP facility...2. Experience and knowledge of standard operating procedures in cGMP laboratory settings. 3. Ability to drive… 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 ....technique, and general lab equipment experience o cGMP , Good Documentation Practices (GDP), or Good Laboratory… 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 +...technique, and general lab equipment experience + cGMP , Good Documentation Practices (GDP), or Good Laboratory… more
- Novo Nordisk (Bloomington, IN)
- …recyclables, autoclaving, ordering, and stocking supplies + Stages materials/components for use within cGMP Quality Control lab + Accurately completes ... room procedure, aseptic technique, and general lab equipment experience + cGMP , Good Documentation Practices (GDP), or Good Laboratory Practices (GLP)… 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 ... execute projects. Provides training support to the manufacturing and quality control teams during tech transfer. +...GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work… 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 and sterility assurance practices for Catalent's aseptic...testing compliance meets the requirements of ISO, USP, CFT, cGMP , and GLP, in the Micro- laboratory at… more
- Honeywell (Baton Rouge, LA)
- …and disposition + Manages and approves cGMP investigations, quality incidents, deviations, CAPAs, change control and out-of-specifications/out-of-trends ... guidelines + Reviews unexecuted and completed batch production and laboratory control records of critical process steps...with internal and external departments to assure compliance with cGMP quality systems and regulations issued by… more
- Eurofins (Indianapolis, IN)
- …or at least 3-5 years of laboratory experience in a cGMP pharmaceutical Quality Control laboratory . + Fundamental knowledge of and experience in a ... Integrity testing laboratory analysts in the Analytical Quality Control Operations (AQCO) organization will serve...operations and must be capable of operating in a cGMP laboratory environment. + Execute approved protocols… more
- Curia (Rensselaer, NY)
- …cGMP regulated industry specific to computer systems validation + Validation experience in a cGMP quality control laboratory or sterile fill finish ... regulations. + Will act as Site System Admin, especially site Quality Control and Manufacturing computerized systems + Generate and execute validation documents,… more
- Curia (Albuquerque, NM)
- …cGMP regulated industry specific to computer systems validation + Validation experience in a cGMP quality control laboratory or sterile fill finish ... 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
- 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 ... role:** + Lead projects within QC Raw Materials + Authors and Executes Quality Records, including Change Controls and Investigations + Sampling of raw materials… 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
- Olon Ricerca Bioscience LLC (OH)
- …and experience is required. Relevant experience in good laboratory /manufacturing practices (GLP/ cGMP ), laboratory quality control or stability, and ... materials, in-process samples, and finished goods in accordance with cGMP /GLP standard operating procedures + May be able to...+ Conduct inspection of the laboratory or laboratory procedures to ensure conformance to internal quality… 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
- Nitto Denko Corp. (Milford, MA)
- … Systems coupled with education and training in Quality Systems, cGMP , Quality audits, documentation, change control , corrective preventative action, ... expert advice and sound decision-making on all aspects of cGMP . + Strong knowledge of the cGMP ...validation, calibration, review of quality records, quality metrics, failure investigations and manufacturing and laboratory… more