Validation Engineer

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

• Execute and/or support equipment qualification activities, including IQ/OQ/PQ.

• 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.