What are the responsibilities and job description for the Analytical Lab Data Reviewer II/III position at WaveCrest Staffing Group?
Our client is seeking experienced Laboratory Data Reviewers II and III to join their team. This is a great opportunity for QC laboratory professionals with strong analytical instrumentation experience to take on a technical, quality-focused role within a GMP environment.
What You’ll Do
What You’ll Do
- Review QC testing and raw analytical data for accuracy, completeness, traceability, and compliance with specifications, SOPs, cGMP, and data integrity requirements.
- Perform technical review of compendial testing (USP/NF, EP, JP), in-house methods, and client-specific methodologies.
- Review data generated from HPLC/UHPLC, GC, ICP-MS, IR, UV-Vis, DSC, Karl Fischer, dissolution, optical rotation, particle size, and other analytical instrumentation.
- Verify calculations, sample/standard/reagent traceability, instrument calibration, usage logs, and GDP compliance.
- Review and trend stability data, prepare stability summaries, and identify unexpected or inconsistent results.
- Support OOS investigations, deviations, CAPAs, change controls, and other Quality Management System activities.
- Review testing performed by external/contract laboratories and coordinate stability sample testing as needed.
- Author, review, and/or approve SOPs, test methods, forms, and other quality documents.
- Collaborate with laboratory personnel, QA, management, and other departments to resolve analytical issues and support client discussions.
- Provide technical guidance and training to new and lower-level Data Reviewers.
- Support raw material release, GMP production suite commissioning, QA inspection/cleaning verification activities, and other quality initiatives.
- Compile and trend laboratory data, prepare management summaries, and identify areas for improvement.
- Several years of QC analytical laboratory experience with hands-on experience using laboratory instrumentation.
- Strong experience with HPLC, GC, UV, IR, particle size, and other analytical techniques.
- Experience working in a GMP/GDP-regulated environment with a strong understanding of data integrity.
- Pharmaceutical experience preferred; biotech, chemical, or other regulated laboratory experience will also be considered.
- Experience with technical data review, stability testing, investigations, CAPAs, deviations, and/or quality systems strongly preferred.