Pharmaceutical Quality Control Validator

5 days ago


Indianapolis, Indiana, United States Verista Full time

The successful candidate will be trained on Deviation Investigation as part of our Entry-level CQV Engineer position in the Pharma industry. With a strong focus on remediation experience, we welcome candidates with undergraduate Engineering/STEM degrees and up to 3 years of experience.

**Key Responsibilities:**

  • CQV Engineer responsibilities include deviation investigation and remediation.
  • Working closely with peers to ensure effective communication and problem-solving.


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