Data Reviewer III

Responsibilities

• Review and approve primary analytical data according to cGMP guidelines.
• Review analytical data including XRPD, PSD, DSC, TGA, UV, FTIR, HPLC, KF, USP testing for compliance and completeness against established SOPs, methods and procedures.
• Support QA initiatives when necessary and collaborate with laboratory personnel to review data per cGMP compliance and data integrity.
• Provide appropriate guidance to analysts, supervisors, and quality personnel to promote compliance for our customers.
• Trend stability data to ensure consistency with historical timepoints and no unexpected results.
• Verify calculations associated with Stability samples/Reference standards/Raw Materials/Intermediates testing are correctly done.
• Format and review Stability summary tables, Stability Protocols for accuracy and compliance with current Curia formats.
• Enter data into Stability summary tables.
• Perform tracking and trending of data as requested.
• Compile data and provide data summaries to management.
• Collaborate with lab personnel for data review per cGMP compliance, data integrity.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and signatures while reviewing electronic data.
• Verify for traceability of samples, standards, reagents, instruments etc.
• Verify the usage logbook, calibration of instruments and shelf life of standards and reagents used are current and GDP procedures are followed.
• Make sure all tests are per cGMP compliance and in compliance with the company’s standard operating procedures.
• Perform electronic review and