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.