Manager - CMQA

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Date: Jan 23, 2026

Location: Airoli, MH, IN

Company: Lupin

Job Description

1. Overall review of QA activities at LL/TP/LLSL sites at Puducherry and

Chennai.

2. Monitoring of process starting from dispensing to packing including

witness analysis of products manufactured under LL/TP/MM arrangement

at contract manufacturing sites.

3. Review of QMS documents (Deviation, Change control, OOS, OOT),

Annual product review reports for products at contract manufacturing

locations.

4. Review of QMS, Process validation, Stability and APQR.

5. Ensuring pharmacopeial compliance and statuary requirement.

6. Periodic audit of Warehouse.

7.Investigation of Market complaints identifying root cause / CAPA and

verification of CAPA effectiveness.

8. Review of new products offered by GSCM. Technology transfer / site

transfer of LL products from own sites to CM sites or from CM site to CM

site.

9. Quality improvement projects (QIP) and other miscellaneous projects

impacting quality of products.

10.Control over the destruction of printed packaging materials at CM sites.

11.Other works assigned by the reporting hierarchy.

Work Experience

Work experience should be 8-11 years, 3 years must be experienced in CMQA role.

Education

Graduation
Post Graduation in Pharmacy or Science

Competencies

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