CQV Consultant

The following website advertisement will be be posted from 05/24/2021 – 06/18/2021

CQV Consultant needed w/Masters degree or Foreign Equivalent in Industrial Engineering or Mechanical Engineering or Systems Engineering and one (1) year experience as CQV Consultant or Quality Engineer performing following job duties or Bachelors degree or Foreign Equivalent in Industrial Engineering or Mechanical Engineering or Systems Engineering and five (5) years of progressive work experience as CQV Consultant or Quality Engineer performing following job duties:

Draw insights from projects and supplemental research to drive new and existing growth.  Develop incoming inspection processes and document incoming inspection activities. Provide in-process QA support to include inspection and document review.   Track nonconforming material and lead Material Review Board (MRB) efforts. Interface with suppliers, contractors and consultants that supply components, subassemblies and contract processing.   Lead complaint investigations on returned product. Perform corrective action and quality improvement activities.  Receive inspection, calibration and MRB.   Assist in the performance of quality system internal auditing. Support quarterly management review meetings. Establish, monitor and evaluate quality system metrics.  Perform document control, training coordination, distribution of documents and other applicable duties.  Perform QMS activities – Document Control, Training coordination and CAPA and Deviation in accordance with procedures.   Support updating QMS systems and perform validation as necessary. Identify and implement improvements to Quality Management System.

Mail Resumes to:
The Veritas Healthcare Solutions LLC
469 7th Avenue, 12th Floor, New York, NY 10018
Job Location: NYC or client sites across U.S.