Job Description

Job Description

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

Chennai.

  • Monitoring of process starting from dispensing to packing including

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

at contract manufacturing sites.

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

Annual product review reports for products at contract manufacturing

locations.

  • Review of QMS, Process validation, Stability and APQR.
  • Ensuring pharmacopeial compliance and statuary requirement.
  • Periodic audit of Warehouse.
  • Investigation of Market complaints identifying root cause / CAPA and

verification of CAPA effectiveness.

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

transfer of LL products from o...

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