Validation Engineer
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Genovice
Indianapolis, IN, US
Summary
The Validation Consultant will execute and support equipment qualification activities including IQ/OQ/PQ for analytical and laboratory instrumentation. They will also develop and review validation protocols and reports while ensuring compliance with GMP and regulatory standards.
Job Description
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
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Execute and/or support equipment qualification activities, including IQ/OQ/PQ.
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Develop and review validation protocols, reports, and associated documentation.
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Support qualification of analytical and laboratory instrumentation/equipment.
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Work closely with Analytical Development, Quality, Engineering, and Validation teams.
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Ensure activities are performed in accordance with GMP requirements and applicable regulatory expectations.
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Previous validation/qualification experience within pharmaceutical, biotech, or other regulated life sciences environments required.
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Strong technical writing and documentation skills.
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Experience with analytical development or QC laboratory equipment strongly preferred.
