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Sr. Executive - CQA

Date:  Mar 6, 2026
Location: 

Airoli, MH, IN

Company:  Lupin

Job Description

Experience in regulatory/customer audits and needs to perform routine/ new site audit of CM location delegated & prepare audit reports.
Review & follow-up for effective compliance of observations made during day-today activities and audits conducted by CQA team.
Implementation of common CAPAs across CM locations.
Hands‑on exposure to sterile/aseptic manufacturing environments, Good understanding of QMS, aseptic practices and compliance systems.
Willingness and ability to travel for audits at various sites.
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.
Preparation and tracking of Quality agreement for API/Intermediate/formulation (US and IRF) CM sites.
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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