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5 days ago · (1) In addition to cases under which debarment action is initiated pursuant to § 5.11, whenever as a result of an investigation conducted by the Federal agency or the Department of Labor, and where the Administrator finds reasonable cause to believe that a contractor or subcontractor has committed violations which constitute a disregard of its obligations to workers or subcontractors under the Davis-Bacon Act, the labor standards provisions of any of the other applicable statutes referenced ...
2 days ago · In depth knowledge of Regulatory Guidelines- USFDA, MHRA, WHO, ISO, 21 CFR part 11 & other regulatory guidelines; Preparations of Commissioning & Qualifications Protocols/ Standard operating Procedures/ Work instructions; as applicable
3 days ago · FDA 21 CFR Part 11: Electronic Records; FDA 21 CFR Part 117: GMP Food Mfg. FDA 21 CFR Part 111: GMP Dietary; Pharmaceutical Sales & Marketing; GLP: Good Laboratory Practice; Clinical Research Training Programs; CRA: Clinical Research Associate; CRC: Clinical Research Coordinator; GCP: Good Clinical Practice Training; Clinical Trial Training ...
4 days ago · FDA 21 CFR Part 11: Electronic Records; FDA 21 CFR Part 117: GMP Food Mfg. FDA 21 CFR Part 111: GMP Dietary; Pharmaceutical Sales & Marketing; GLP: Good Laboratory Practice; Clinical Research Training Programs; CRA: Clinical Research Associate; CRC: Clinical Research Coordinator; GCP: Good Clinical Practice Training; Clinical Trial Training ...
2 days ago · In depth knowledge of Regulatory Guidelines- USFDA, MHRA, WHO, ISO, 21 CFR part 11 & other regulatory guidelines; Preparations of Commissioning & Qualifications Protocols/ Standard operating Procedures/ Work instructions; as applicable
3 days ago · Responsible for onsite support C&Q activities by following ISPE/ASTM methodologies utilizing GDP, GEP, C&Q Base line guides, GAMP 5 & cGMP Principles. Planning, developing, execution, reporting of C&Q Deliverables. Coordination with different package design engineers & Clients, Project managers to enable effective leveraging and timely Right ...
3 days ago · In depth knowledge of Regulatory Guidelines- USFDA, MHRA, WHO, ISO, 21 CFR part 11 & other regulatory guidelines; Preparations of Commissioning & Qualifications Protocols/ Standard operating Procedures/ Work instructions as applicable
