Sr. Executive - CQA

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Date: Mar 6, 2026

Location: Airoli, MH, IN

Company: Lupin

Job Description

Review of documents such as executed Batch Production Records, Analytical records, Change Controls, Deviations, OOS, process Validation, Cleaning Validation, Equipment Qualification, stability data and CAPA for IRF Market and US formulation CM sites.
Routine/ new site audit of CM location delegated& prepare audit reports.
Implementation of common CAPAs across CM locations.
Review & follow-up for effective compliance of observations made during day-today activities and audits conducted by CQA team.
Preparation and tracking of Quality agreement for API/Intermediate CM sites.
Provide monthly update on the QMS activity and preparation of Monthly report.
Review & implementation of Pharmacopeial changes for products.
Review of new products offered by GSCM.

Work Experience

4 - 5 years of expereince in the CMQA Role.

Education

Graduation
Post Graduation in Pharmacy or Science

Competencies

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