Validation Engineer

Genovice; Indianapolis (IN); On-site; USD 90,000 - 120,000; Full time

Job summary

Genovice is seeking an experienced Validation Consultant to support qualification and validation activities for analytical development and laboratory equipment within a regulated pharmaceutical environment.

Location: Indianapolis, IN. Engagement: Contract. You will develop and review validation protocols and reports, qualify analytical instrumentation, and collaborate with Analytical Development, Quality, Engineering, and Validation teams to ensure GMP compliance and regulatory expectations.

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.
• Strong technical writing and documentation skills.
• Experience with analytical development or QC laboratory equipment strongly preferred.

Responsibilities

• 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.
• Strong technical writing and documentation skills.
• Experience with analytical development or QC laboratory equipment strongly preferred.

Job description

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

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

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.