Summary
ProPharma is seeking deviation writers to support quality control activities for pharmaceutical and biotech clients. You will complete required training, participate in meetings, and clearly communicate progress on deviation records.You will own records through approval, conduct root cause investigations, and develop CAPAs with effectiveness checks. The role requires experience in Quality Control Laboratories, familiarity with Veeva QMS or similar systems, LabVantage, and strong written#J-18808-Ljbffr
Job Description
ProPharma is seeking deviation writers to support quality control activities for pharmaceutical and biotech clients. You will complete required training, participate in meetings, and clearly communicate progress on deviation records.You will own records through approval, conduct root cause investigations, and develop CAPAs with effectiveness checks. The role requires experience in Quality Control Laboratories, familiarity with Veeva QMS or similar systems, LabVantage, and strong written#J-18808-Ljbffr
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