Apply now »

Executive

Date:  May 27, 2026
Location: 

Goa, GA, IN

Company:  Lupin

Job Description

  • Design, Preparation and Review of documents related to manufacturing – Pas-X BMR’s for Scale up, Exhibit, Intended and Commercial manufacture of products, qualification, verification protocols, reports and MFC.
  • Preparation and Review of Experimental batch report and scale up batch report.
  • Compilation of batch data and preparation of Test Batch Validation / Monitoring Protocols (or) Reports and Process Validation Protocols (or) Reports.
  • To initiate and review change controls, incidents, deviations, CAPA, IPOOS, OOS, OOT, OOE, market complaints and other QAMS related activities.
  • Execution and co-ordination for SAP related activities like loading of Masters of Semi Finished Goods (SFGs), Recipes and Bill of Materials (BOMs), for Semi Finished Goods (SFGs).
  • Preparation and review of stability protocols for Experimental batches / Exhibit / Commercial Products / Intended commercial production.
  • Prepartion of QRMs, Nitrosamine risk assesmemt, Regulatoru query response related to process development related query. 
  • Participation in self-inspection as auditees and compliance of the self-inspection observations.

 

Work Experience

5 to 8 years 

Education

Graduation in Pharmacy
Masters in Pharmacy

Competencies

Customer Centricity
Developing Talent
Collaboration
Strategic Agility
Process Excellence
Stakeholder Management
Innovation & Creativity
Result Orientation

Apply now »