- Verista (Durham, NC)
- …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 (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
- Verista (The Woodlands, TX)
- …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...IQ, OQ, PQ Requirements + 5-7 years of demonstrated CQV experience in GMP regulated (preferably Cell and Gene… 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)
- …cGMP's, and regulatory standards to support team in compliance of validation effort + Independent verification of testing against specifications + Managing ... + Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as… more
- Verista (Indianapolis, IN)
- …+ Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as ... schedule for all assigned activities. + Maintaining clear, detailed records qualification and validation + Documenting impact and risk assessments as part of a team.… more
- VTI Life Sciences (Los Angeles, CA)
- …of the biggest companies in the Life Sciences industries. We are looking for a CQV Engineer with 5+ years of experience in Project Engineering and Validation ... for a 2-year project to help support Engineering and CQV activities related to the project expansion at our client's pharmaceutical facility in the Greater Los… more
- Verista (Indianapolis, IN)
- …New College Grad Opportunity! + Change Control Support (TrackWise): author, monitor, and ensure closure by Target Due Date: + Initiating impact analysis meetings and ... task development. + Develop/write required change controls and implementation steps with information obtained from the Impact Assessment(s). + Submitting change controls to appropriate personnel for review - make modifications/updates based on feedback and… more
- VTI Life Sciences (Los Angeles, CA)
- …Specialist/ Engineer 1 responsible for delivering commissioning, qualification, and validation ( CQV ) services related to equipment, instruments, and systems ... a VTI employee, you will continue to learn and implement industry-standard methods for CQV (ISPE Baseline Guide, ASTM E2500) and temperature mapping in a GxP (good… 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
- Takeda Pharmaceuticals (Social Circle, GA)
- …my knowledge. **Job Description** **About the role:** Join Takeda as a Senior Validation Engineer where you will support site projects, technical transfers, and ... regulated environment. + At least 4 years of commissioning, qualification and validation ( CQV ). + Validation and system experience in the following… more
- Gilead Sciences, Inc. (Frederick, MD)
- …**Responsibilities:** + Provide Quality Engineering oversight for Commissioning, Qualification, and Validation ( CQV ) related activities. + Represent site in ... motivated individual to join us as a Sr Quality Engineer I, reporting to the Associate Director, Quality Engineering...global matrix team towards strategic CQV alignment, and corporate CQV goals. +… more
- ThermoFisher Scientific (Plainville, MA)
- …or Biological science related field preferred + 5 years experience in CQV (Commissioning, qualification and validation ) + Meaningful work experience in ... Schedule** Other **Environmental Conditions** Office **Job Description** **Position summary** Validation engineers **lead, inspect, calibrate, test and modify the… 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
- ThermoFisher Scientific (Cambridge, MA)
- **Job Description** **DUTIES:** Plan and execute validation projects including working with the Thermo Fisher core teams to understand the scope of validation ... revisions, providing input, as necessary; Coordinate with stakeholders for validation project initiatives, including protocol generation, execution and closeout;… 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
- VTI Life Sciences (Los Angeles, CA)
- …We are looking for Two (2) Facilities Engineers to help support engineering and CQV activities related to equipment and systems affected by the project expansion at ... + 5+ years of relevant FDA regulated industry experience as a Facilities Engineer . + Knowledge of cGMP and other regulatory standards. + Stakeholder management… more
- Nestle (Schaumburg, IL)
- …and validate electricity and automation requirements. + Participate in Commissioning, Qualification, Validation ( CQV ) + Contribute to the project close out, ... position is not eligible for Visa Sponsorship._ The E&A Engineer will lead the design and implementation of electrical,...capital projects that require electrical engineering expertise. The E&A Engineer will act as the site's expert on all… more
- Verista (Indianapolis, IN)
- …learn from our experiences to enhance our collective expertise Senior CSV Engineer /Analyst Responsibilities: + Provide IT CSV support to implement and validate ... issues/escalations and other metrics/KPIs + Work directly with the business, validation team and other stakeholder groups for implementation, operational and… 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