- Verista (Indianapolis, IN)
- …of an electrical engineer + Bachelor's Degree or equivalent required. + 2 -4 years of applicable industry experience + Proficiency using PC and Microsoft Office ... cGMP's, and regulatory standards to support team in compliance of validation effort + Independent verification of testing against specifications + Managing… more
- Verista (Columbus, OH)
- …new skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: This role will require supporting the client in ... Columbus, Ohio. Resource will be required to draft validation and commissioning documentation including, change requests, system impact assessments, user requirement… more
- Actalent (Durham, NC)
- Description: Joining a collaborative team providing Commissioning, Qualification, and Validation ( CQV ) support to manufacture GMP products. * Executing CQV ... and resolving protocols exceptions or anomalies, developing technical reports, and CQV summary reports. * Developing Scientific and Engineering studies to support… more
- Verista (Indianapolis, IN)
- …from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: * Manage the validation and documentation related to complex ... pieces of equipment/large upgrades/extensive product updates * Perform functions of validation engineer - draft Validation Plans, Requirements, Test Cases,… more
- Verista (Kalamazoo, MI)
- …skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: This role will require supporting the client site ... in Kalamazoo, MI. Resource will be required to draft validation and commissioning documentation including, change requests, system impact assessments, user… more
- Verista (Fishers, IN)
- …technical precision; and consistent use of independent judgment and discretion. Kneat Validation Engineers utilize Kneat Gx and CSV/ CQV experience to provide ... implement this knowledge at a client + Direct experience authoring/editing/executing validation documents + Can demonstrate the Functional Differences between a… more
- VTI Life Sciences (Los Angeles, CA)
- …looking for Two ( 2 ) Facilities Engineers to help support engineering and CQV activities related to equipment and systems affected by the project expansion at our ... + 5+ years of relevant FDA regulated industry experience as a Facilities Engineer . + Knowledge of cGMP and other regulatory standards. + Stakeholder management… more
- Actalent (Durham, NC)
- Job Title: Automation EngineerJob Description As an Automation Engineer , you will use your proven knowledge of Rockwell Automation/Allen Bradley Hardware and ... Your responsibilities will range from serving as the principal automation engineer during the startup phase, extracting technical data, supporting development of… more
- BeiGene (Hopewell, NJ)
- …regulatory compliance and achieving commercial success. Reviews, authors and works with CQV validation of start-up Green-Field Project. Works with Drug ... required to work closely with both manufacturing, quality, and engineer associates. + Maintaining the validation sample...of cGMP and Data Integrity principles. + Minimum of 2 years' experience in metrology and CMMS management. +… more