Validation Engineer
-
Pharmaceutical
Job Description & How to Apply Below
Indianapolis, United States | Posted on 09/23/2026
- Industry Pharma/Biotech/Clinical Research
- Work Experience 5+ years
- City Indianapolis
- State/Province Indiana
- Country United States
Validation Consultant – Analytical Development Equipment
Location: Indianapolis, IN
Engagement: Contract
Industry: Pharmaceutical / Radiopharmaceutical Manufacturing
Genovice is seeking an experienced Validation Consultant to support qualification and validation activities for analytical development and laboratory equipment within a regulated pharmaceutical environment.
Key Responsibilities & Qualifications
Develop and review validation protocols, reports, and associated documentation.
Support qualification of analytical and laboratory instrumentation/equipment
.
Work closely with Analytical Development, Quality, Engineering, and Validation teams.
Ensure activities are performed in accordance with GMP requirements and applicable regulatory expectations
.
Previous validation/qualification experience within pharmaceutical, biotech, or other regulated life sciences environments required.
Strong technical writing and documentation skills.
Experience with analytical development or QC laboratory equipment strongly preferred.
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