Analytical Validation Specialist – Pharma Equipment

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

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.