Division
ANKLESHWAR QA -U1
Job posted on
Feb 23, 2026
Employee Type
P-P8-Probationer-HO Executive
Experience range (Years)
0 - 0
Ensure compliance with GMP, safety norms, company policies, and Positive Laboratory Practices (GLP).
Review and approve analytical reports for intermediates, APIs, drug substances, stability studies, and instrument calibration.
Oversee Unit‑II stability and API reports, working/reference standards, and Certificates of Analysis (COA).
Manage laboratory incidents, out‑of‑calibration investigations, and controlled QC documentation.
Review continuous process verification data, audit trails in laboratory software, and user access privileges.
Conduct pharmacopoeia evaluations, specifications,



and standard testing procedures.
Coordinate documentation for Drug Master File (DMF) filings.
Validate laboratory instruments, equipment, and software systems.
Support technology transfer, change management, and risk assessment activities.
Review trend analysis reports, stability summaries, miscellaneous protocols, and training evaluations.
Initiate, track, and close Corrective and Preventive Actions (CAPA) in Trackwise.
Collaborate with cross‑functional teams to ensure regulatory readiness and continuous improvement.

📌 Qa Of Qc Ankleshwar (India)
🏢 Zydus Group
📍 India