Validation Engineer

Genovice
  • Indianapolis, Indiana
  • Autofill and Review
30+ days ago

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

  • 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.

Numbers & Facts

LocationIndianapolis, Indiana

Skills

  • Analytical Developmentunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Consultingunmatched
  • Documentationunmatched
  • Drug Manufacturingunmatched
  • Environmental Sciencesunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Instrumentationunmatched
  • Laboratory Equipmentunmatched
  • Process Validationunmatched
  • Quality Controlunmatched
  • Quality Engineeringunmatched
  • Regulationsunmatched
  • Technical Writingunmatched
  • Validation Planunmatched
  • Writing Skillsunmatched

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