Management System Jobs in Juncos
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Capa Complaints Technical Writer
Qrc Group, Llc
The CAPA / Complaints Technical Writer is responsible for authoring reviewing and maintaining high-quality documentation associated with Corrective and Preventive Actions (CAPA) customer complaints investigations non conformances and Quality Management System (QMS) remediation activities within a re...
Manager Information Systems
Hitachi
Location:Ludvika Dalarna County SwedenJob ID: R0103717Date Posted:Company Name:HITACHI ENERGY SWEDEN ABProfession (Job Category):IT Telecom & InternetJob Schedule:Full timeRemote:NoJob Description:The opportunityIn the role as Manager Information Systems you oversee Information Systems for HVDC on...
Qa Specialist 35383 Microbiology
Integrated Services For Productivity & Validation, Inc
Knowledge in: Environmental Monitoring Microbial Identification (Micro ID) Critical Utilities (CU) monitoring Sampling monitoring: equipment and techniques Data trending and evaluation Microbiological testing methods and standards for clean rooms and controlled environments Aseptic behavior in manuf...
Specialist Manufacturing 35321
Integrated Services For Productivity & Validation, Inc
Experience in the Manufacturing area specifically writing procedures managing documents in management system (document workflow)RequirementsDoctorate degree OR Masters degree and 3 years of Manufacturing Operations experience Alternatively Bachelors degree and 5 years of Manufacturing Operations exp...
Specialist Qa 35327 Juncos 500pm-530am
Integrated Services For Productivity & Validation, Inc
Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...
Qa Specialist Shft 5 Pm To 530 Am 35165
Integrated Services For Productivity & Validation, Inc
Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...