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# Data Reviewer, Analytical Development

- **Company:** Arrowhead Pharmaceuticals
- **Location:** Pasadena, CA, United States
- **Experience:** Experienced
- **Salary:** $80,000.0 - $90,000.0
- **Contract:** Permanent contract
- **Skills:** Software Documentation, Data Integrity, Fourier Transform Infrared Spectroscopy, Laboratory Information Management Systems, Model Validation
- **Published:** July 17, 2026
- **Apply:** https://www.dice.com/job-detail/d2a237dd-0745-4b30-a2a5-3975c626d81e

## About the Role

* Bachelor's degree in chemistry or (any STEM degree) and 5+ years GMP experience, or a Master of Science (STEM degree) with minimum 3 years of experience in a cGMP laboratory (pharmaceutical CMO/CRO).
 * Experience with analytical data review and documentation practices
 * Working knowledge and experience with chemistry analytical methods such as HPLC, LC-MS, NMR, FTIR, Appearance, pH, KF, UV spectrometry and microbiology testing.
 * Working knowledge of GMP/GDP and laboratory systems

Preferred

 * Working knowledge of USP, ISO, FDA and ICH guidelines
 * Familiarity with laboratory information systems, LIMS.
 * Strong verbal and written communication skills and ability to work with diverse professionals in a matrix environment.
 * Solid organizational skills with ability to adapt to changing priorities and deadlines.

## Description

The Data Reviewer independently performs technical review of laboratory data and documentation to ensure compliance with analytical methods, specifications, GMP/GDP requirements, and data integrity standards. This role exercises independent judgment in evaluating data quality, identifying discrepancies, and resolving routine to moderately complex compliance issues. The Data Reviewer supports inspection readiness activities, contributes to continuous improvement initiatives, and serves as a technical resource to junior team members., * Perform independent technical review of internal data and external laboratory data

 * Evaluate data for accuracy, completeness, and compliance with GMP and specifications
 * Independently evaluate, investigate, and document discrepancies, atypical results, and documentation inconsistencies to determine impact and ensure appropriate resolution
 * Review routine release and stability data, method validation data and report, IPC data, cleaning samples, and logbooks for traceability and compliance
 * Communicate and collaborate with laboratory staff and CDMOs to resolve data quality issues
 * Support audit readiness activities and participate in inspections
 * Maintain knowledge of laboratory systems and software for effective review
 * Recommend and support implementation of improvements to data review processes, documentation practices, and workflow efficiency
 * Provide guidance and onboarding support to junior reviewers on review practices, documentation standards, and GMP expectations
 * Embrace digital tools and opportunities for trend analysis, system suitability trending.
 * Perform additional duties as assigned in support of operations


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