- Cedars-Sinai (CA)
- …in accordance with SOPs. + Follows Current Good Manufacturing Practices ( cGMP ). **Qualifications** **Position Requirements:** + Baccalaureate Degree in a biological ... science, chemistry, medical technology, or related science. + Valid California Clinical Laboratory Scientist license or limited license appropriate for the area of responsibility. + Five (5) years of relevant clinical experience with at least one (1) year in… more
- Herbalife (Lake Forest, CA)
- …to the specific functions of inventory system. * Working experience in a cGMP facility * Experience working in a warehouse with material handling equipment and ... conveyance **PHYSICAL DEMANDS:** In general, the following physical demands are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to allow otherwise… more
- Kelly Services (Petaluma, CA)
- …field required. + 5+ years of industry experience within a cGMP manufacturing cleanroom facility. + Proven experience authoring procedures for microbiological ... analyses and performing test method validations on analyses, such as paraben, preservative, and bioburden testing ( _USP 61, 51)._ + Knowledge and experience in environmental monitoring and Biosafety Level 1 and 2 laboratory protocols + Knowledge of GMP and… more
- Fujifilm (CA)
- …right place for you. From our Bioprocess Innovation Center to our cGMP -compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether ... your expertise lies in research, manufacturing, or production, you'll find a home here where your efforts directly improve patients' lives. Together, let's shape the future of healthcare. Situated at the cross-section of Morrisville and Research Triangle Park… more
- Belcan (City Of Industry, CA)
- …stacking, and material handling. * Detailed cleaning of equipment/facilities to MSP/ cGMP standards. * Complete technical training profile as required. * Strict ... adherence to Dept. Safety Rules and GMP compliance. * Perform real-time accurate documentation during the production run. * Working experience of Level 1 Packaging Equipment, ie Shrink Bander, Labeler, Cartoner, and Case Sealer. * Receive product and material… more
- ManpowerGroup (Rocklin, CA)
- …+ Review submitted document change requests to ensure compliance with established cGMP and related standards. + Assist in processing documentation changes in the ... document control system, ensuring timely and accurate updates. + Support Document Control department activities and perform additional administrative duties as needed. **What's Needed?** + A minimum of a 2-year degree; a 4-year Bachelor's degree is preferred.… more
- Catalent Pharma Solutions (San Diego, CA)
- …on 1st shift. The Manufacturing Technician I will be responsible for conducting cGMP manufacturing of solid oral and liquid oral pharmaceutical dosage forms for ... Phase I and Phase II clinical trials. Under the direction of the Manufacturing Supervisor or Team Lead, the Manufacturing Technician will work hands on, in their designated production suite, with a variety of manufacturing production equipment and… more
- Catalent Pharma Solutions (San Diego, CA)
- …for product release. Determines if records are compliant with internal and cGMP (Good Manufacturing Practices) regulations + Liaison between Manufacturing and QA for ... executed Batch Record Review and flow of documents + Liaison between QA and client and effectively communicates with clients in regards to Executed Batch Records (EBR) and review status + Tracks status of Executed Batch Records and maintains established… more
- Bayer (Berkeley, CA)
- …Degree in a science or technical field. * Demonstrable experience with cGMP and regulatory compliance (FDA, EMA and other international agencies). * Ability ... to support and prioritize many diverse activities simultaneously while meeting schedule commitments. * Thorough knowledge of microbiological analytical methods, compendial requirements (USP, EP, JP), ACS and FCC requirements. Knowledge of biologics and… more
- VTI Life Sciences (San Diego, CA)
- …writing, review and analytical skills. + Knowledge of good documentation practices and cGMP . SALARY RANGE FOR THIS ROLE IS $80,000 - $105,000 ANNUALLY FOR A ... W2 EMPLOYEE VTI Life Sciences strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device… more