- 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 (Germantown, WI)
- …and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Managing the responsibilities on multiple simultaneous ... point of escalation and issue management on client projects + Designing validation plans + Designing and executing engineering studies for critical process parameter… more
- Verista (Lexington, MA)
- …skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: + Authoring, editing, and executing technical ... commissioning, qualification and validation documentation for (FAT, SAT, etc) and execution for...experience with Data Integrity + Demonstrated experience in leading CQV activities specific to Process Equipment + Proficiency using… more
- Verista (Germantown, WI)
- …new skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: + Managing and working collaboratively with clients' ... + Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as… more
- Verista (Kalamazoo, MI)
- …skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Designing validation plans. + Conducting ... the team maintains) clear, detailed records of qualification and validation , and change control activities for future compliance audits...onsite in Kalamazoo, MI + 5-7 years of demonstrated CQV experience in GMP regulated (preferably Cell and Gene… 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
- 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