- Amgen (New Albany, OH)
- …work nonstandard shifts to support 24/7 operations. + Experience in an FDA ( GMP ) or comparable regulated environment preferably Pharmaceutical and/or ... instrumentation, and control systems. + Perform required work in a GMP regulated manufacturing setting. + Implement Preventative and Corrective maintenance. +… more
- Endo International (Rochester, MI)
- …in a body of information required for the job_ _e.g. knowledge of FDA regulations, GMP /GLP/GCP, Lean Manufacturing, Six-Sigma, etc._ + Review and evaluate ... field with 6+ years' laboratory experience in QC functions in a GMP laboratory + Data Integrity assessment experience + Direct experience authoring/editing/executing… more
- Robert Half Finance & Accounting (Morristown, NJ)
- …as Pharmaceutical Sciences, Chemistry, or a related discipline. * Strong knowledge of FDA GMP regulations and quality management systems. * Proven ability to ... and driving quality management initiatives. Responsibilities: * Ensure adherence to FDA Good Manufacturing Practices ( GMP ) and other regulatory standards… more
- ADM (Northwood, ND)
- …to final destination (rail cars or bagging). + Maintains awareness and adheres to all FDA , GMP , BATF, EPA, OSHA and employer standards and guidelines. + Suggests ... safety is everyone's responsibility + Maintains awareness and adheres to all FDA , GMP , BATF, EPA, OSHA and employer standards and guidelines. + Suggests… more
- Aerotek (Cleveland, OH)
- …Compliance Administrator to adhere to good production practices and meet HACCP, FDA , GMP , and OSHA standards, including daily paperwork checks. ... product weights. + Communicate product substitutions effectively. + Adhere to HACCP, FDA , GMP , and OSHA standards. **Essential Skills** + At least 2 years of… more
- Kelly Services (Orange County, CA)
- …processes across multiple projects. + Ensure strict adherence to **industry regulations** (eg, FDA , GMP , ISO) and **company policies** . + Conduct **regular ... , or **manufacturing** industries. + Strong knowledge of **regulatory guidelines** (eg, FDA , GMP , ISO) and industry best practices. + Exceptional… more
- Danaher Corporation (Richmond, IL)
- …Authorized Representative actions. + Experience with ISO 13485:2016, IVD/MDR Regulations, FDA GMP and domestic/international Medical Device Regulations. It would ... Subject Matter Expert (SME) in site audits (ie MDSAP, GMP , MAPSS, etc.). + Support product registrations, listings, and...Minimum of two years' experience within medical device/IVD. + FDA (Class I & II) and Health Canada regulatory… more
- Abbott (San Diego, CA)
- …and monitor effectiveness of engineering systems and procedures to ensure compliance to FDA , GMP and all other applicable agency regulations + Anticipate and ... requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes,… more
- ADM (Decatur, IL)
- …analytical results in a timely matter. + Support and comply to all applicable FDA , GMP , USP, Biosafety, and OSHA requirements. + Follow laboratory standards and ... applications, and software). + Maintain awareness and adhere to all applicable FDA , GMP , USP, Biosafety, OSHA and employer standards and guidelines. + Follow… more
- Abbott (Houston, TX)
- …train and monitor effectiveness of engineering systems and procedures to ensure compliance to FDA , GMP , and all other applicable agency regulations. + Ensure a ... environment. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes,… more