JOB RESPONSIBILITIES :
To ensure GMP compliance, Laboratory compliances and inspection readiness at site.
Review of all Analytical data generated at laboratory during testing.
Review of audit trail of QC instruments as per define schedule.
Verification of electronic data generated at laboratory during testing.
Review and approval of Method Feasibility / Verification / Validation / Transfer protocol, Record of analysis and reports.
Review and approval of Calibration documents, Certificates.
Carry out laboratory activities through LIMS software as per relevant procedure.
Review and approval of Analyst Qualification data.
Review of chromatography data and perform electronic signature.
Review of working standard qualification data.
Review of volumetric solution preparation, reagent, Indicator, SST solution and colorimetric solution data.
Review and approval of Stability summary report.
Review and approval calibration/Preventive maintenance schedule.
Review and approval calculation sheets.
Create and Review of Instrument method in respective Quality control Instruments.
To perform all laboratory activities as per existing SOPs, IOCP’s and GTP’s.

📌 Aqa, Senior Executive Vadodara
🏢 Alembic Pharmaceuticals
📍 Vadodara