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On-site

Job Type

Full Time

Job Description

Job Location :


About the Company :


Company

About Us

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.


About the Role :


To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.


Responsibilities :


  • To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
  • Technology transfer of developed products to plant level, this includes all TTD-related works.
  • To collect and compile all data and submit to respective regulatory agencies.
  • To address DCGI/ regulatory agency queries as per requirement.
  • To extend support to plant for any commercial trouble shooting.

Qualifications :


Ph/D


Required Skills :


  • Formulation Development

    (solid oral dosage forms: tablets, capsules)
  • Pre-formulation Studies

  • Bioequivalence Study Design & Evaluation

  • Technology Transfer (TTD)

  • Scale-Up and Commercialization

  • Analytical Data Interpretation

  • Process Optimization & Troubleshooting

  • Stability Studies (ICH Guidelines)

  • Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)

  • Quality by Design (QbD)


Preferred Skills :


Hands-on Experience with Formulation and Development


Pay range and compensation package :


8 LPA to 12 LPA

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Cadila Pharmaceuticals Limited logo
Cadila Pharmaceuticals Limited

Pharmaceuticals

Ahmedabad

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