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Cadila Pharma

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Deputy Manager

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Description

JOB RESPONSIBILITIES

  • Review of Literature summary report, patent summary report and development protocols.
  • New product development, Planning and Resource allocation for Domestic, ROW, US, EU, CMO

Market.

  • Alternate source development for API and Excipients, GC improvement of existing products.
  • Timely execution of scale up/ exhibit/process validation of allotted projects.
  • Process improvement and troubleshooting of existing commercial products.
  • Overall review of Formulation Development data during stage gate clearance.
  • Execution of allotted projects in stipulated timeline & within budget.
  • To check feasibility of manufacturing and costing of all new projects for UID.
  • Timely review of LNB and project files for allotted projects.
  • To coordinate with CFT team like AR Lab, Production, Manufacturing, QA/QC for timely

completion of project.

  • Ensure timely address of regulatory deficiencies for Domestic, ROW, US, EU, and CMO Products.
  • Compilation and review of the FnD data, interpretation and summarize the recommendations.
  • Preparation and Review of technical documents such as MFC, SOP, PDR, TTD protocol, MMD, FPS and development protocol.
  • Ensuring the availability of manufacturing and analytical requirements/documents and resources before execution of batches at plant.
  • To evaluate the deviations noticed during technology transfer at shop floor and perform root cause analysis and rectification after consultation with the concerned department.
  • Ensure adherence to guideline in various product development activities during development

Skills

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