The following website advertisement will be posted from
04/19/2021 – 05/07/2021
CQV/CSV Validations needed w/Masters degree or Foreign Equivalent in Biotechnology or Biomedical Engineering or Biological Sciences and one (1) year experience as CQV/CSV Validations or Quality Engineer performing following job duties or Bachelors degree or Foreign Equivalent in Biotechnology or Biomedical Engineering or Biological Sciences and five (5) years of progressive work experience as CQV/CSV Validations or Quality Engineer performing following job duties:
Generate and execute life cycle documentation (FAT, SAT, IOQ, PQ) for cleaning, shipping, facilities, utilities, systems, equipment, and processes for (re)qualification/ (re)verification. Perform QMS activities such as Document Control, Training coordination, CAPA, Deviation in accordance with procedures. support internal audits, CAPAs, measure the effectiveness of the QMS, read and interpret Piping and Instrument Diagrams (P&IDs), and electrical diagrams executing protocols including systems such as Process Validation, utilities, manufacturing equipment and laboratory validation. Write procedures, investigations, protocols, reports change controls to support the Maintenance and Engineering departments. Write and execute protocols, resolve deviations/ discrepancies, review and analyze study data, writes summary reports. Perform P&ID Walkdowns. Perform Thermal mapping of temperature-controlled chambers, warehouses, and SIP processes.
Mail Resumes to:
The Veritas Healthcare Solutions LLC
469 7th Avenue, 12th Floor, New York, NY 10018
Job Locations:
NYC or client sites across U.S.
Must be available to travel and relocate to client sites.
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