- 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
- 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
- Verista (Indianapolis, IN)
- …+ 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 review comments. +… 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
- 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
- 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
- Takeda Pharmaceuticals (Social Circle, GA)
- …in a GMP regulated environment. + At least 4 years of commissioning, qualification and validation ( CQV ). + Validation and system experience in the following ... Description** You will support site projects, technical transfers, and ongoing validation maintenance on-site at our Covington Georgia facility. You will report… 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
- 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
- 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
- Insight Global (Plainville, MA)
- …DeltaV. - Experience reviewing and supporting the execution of Commissioning, Qualification and Validation ( CQV ) Activities. null We are a company committed to ... Job Description Insight Global is seeking a Automation Engineer III to join one of our top pharmaceutical clients in Plainville, MA. This individual will be… 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 ... will be required to work closely with both manufacturing, quality, and engineer associates. + Maintaining the validation sample management, assessing the… more
- VTI Life Sciences (Los Angeles, CA)
- …We are looking for Four (4) Project Engineers to help support engineering and CQV activities related to equipment and systems affected by the project expansion at ... + Coordinate with cross-functional departments including but not limited to Validation , Manufacturing, Quality, Supply Chain, and Engineering. + Support FMEA… more