Executive

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Date: Nov 18, 2025

Location: Goa, MH, IN

Company: Lupin

Job Description

  1. Comply with all cGMP, GxP or any other regulatory requirements including EH&S requirements.
  1. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
  1. Conduct all tasks/ activities as per the applicable SOPs. Report any difficulty or deviation in following the procedures/instructions to immediate Supervisor/Managers.
  1. Report any quality concerns or suggestions for improvements to Supervisors/Managers.
  1. Responsible to complete the assigned trainings, applicable for workgroup “PDL-Personnel -GOA” in the L2LMS (SABA).
  1. Scale up of the product manufacturing process, which involves Process Development and Process Optimization.
  1. Monitoring of Pre-Exhibit, exhibit, confirmatory and process validation batches on production floor.
  1. To check the raw material status required for scale-up and Exhibit batches.
  1. To assist in technology transfer of the new and existing products.
  1. Document and Record Management.
  1. Preparation and issuance of placebo batches.
  1. Issuance of Requisition for raw and packing material for trial, experimental and placebo batches.
  1. Preparation and Review of Trial batch report and scale up batch report.
  1. Design, Preparation and review of documents related to manufacturing – BMR’s for scale up, exhibit, Intended and commercial manufacture of products, qualification, verification protocols and reports, sampling plan, MFC and Preparation of Formulation and Process Related Risk Assessment.

Work Experience

1-4 years.

Competencies

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

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