Aristo Pharmaceuticals – Sikkim | Hiring for Lab QA
Designation: Officer / Senior Officer
Department: Lab QA
Qualification: B. Pharm / M. Pharm / M.Sc.
Location: Sikkim
Job Profile – Lab QA
Responsible for review and verification of QC analytical data, calculations, chromatograms, spectra, and analytical records for batch release.
Responsible for review and evaluation of OOS/OOT, deviations, incidents, investigations, and CAPA related to laboratory activities.
Responsible for stability program management, including review of stability protocols, reports, data, and trend analysis.
Review of analytical method validation/verification, method transfer, instrument qualification/calibration, and related laboratory documentation.
Ensure compliance with GMP, ALCOA+ and Data Integrity requirements in QC laboratory activities.
Responsible for preparation/review of SOPs, protocols, reports, and other Lab QA documents, along with support during regulatory/customer audits.
Interested candidates can share their updated resume at:
vishal.chanday@aristopharma.co.in
Sailesh.Rai@aristopharma.co.in
