Data Integrity Analyst - GMP & Compliance

Curium Pharma; Noblesville (IN); On-site; USD 70,000 - 100,000; Full time

Job summary

Curium Pharma in Noblesville, IN is seeking a contractor to provide Data Integrity support for electronic and equipment systems at our Noblesville facility. The role follows a Monday - Friday 8am - 4:30pm schedule, focusing on ensuring data integrity across manufacturing and laboratory environments.

Responsibilities include reviewing documentation, conducting system assessments, and ensuring compliance with US and international data integrity regulations.

Qualifications

• Bachelor degree preferred; work experience is considered in lieu of degree.
• 3+ years of experience understanding and interpreting cGMP/GLP/GCP with a focus on Data Integrity.
• Experience reviewing or authoring standard operating procedures (SOPs).
• Proficiency with core software: Word, Excel, SharePoint, Project.

Responsibilities

• Review system documentation (user manuals, SOPs, validation reports).
• Conduct system assessments and inspections.
• Analyze audit trails for evidence of data manipulation, deletions, or unauthorized access.
• Review data for completeness, accuracy, and consistency.
• Assess data backup and recovery procedures.
• Evaluate user access controls and permissions.

Skills

Data Integrity

cGMP knowledge

Data Analysis

Education

Bachelor's degree preferred

Tools

Microsoft Word

Excel

SharePoint

Project

Job description

Curium Pharma in Noblesville, IN is seeking a contractor to provide Data Integrity support for electronic and equipment systems at our Noblesville facility. The role follows a Monday - Friday 8am - 4:30pm schedule, focusing on ensuring data integrity across manufacturing and laboratory environments.

Responsibilities include reviewing documentation, conducting system assessments, and ensuring compliance with US and international data integrity regulations.