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Bachelor's Degree in Chemical, Electrical, Biomedical, or related Engineering field.
2-5 years of CQV experience in the pharmaceutical or Biotech industry
Skills in IO & loop check qualification protocols post review closure followup, DeltaV coding qualification deliverable site execution , pre-post execution document author
Strong understanding of GAMP 5, S88/S95 standards, and 21 CFR Part 11
Direct experience with Emerson DeltaV.
Ability to manage multiple open loops and drive vendors/contractors to document closure.
Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills.
Job ID: 142814737