Job Description

  • Prepare, Review and Finalize Regulatory strategies for Complex Products [like injectables that may include Peptides, Microspheres, Liposomes, Nano-suspensions etc./ Ophthalmic/ Otic/ Topical gel/ DDCP etc.] and 505(b)(2) Products for US and EU market.
  • Draft, Review and Finalize Pre-ANDA/Pre-IND/ScA meeting packages for US and EU market.
  • Draft and finalize controlled correspondences on complex issues.
  • Draft, Review and Finalize Deficiency responses for Complex Products and 505(b)(2) Products.
  • Review API and FP in-vitro characterization/sameness reports.
  • DMF review for complex APIs as per the workflow.
  • To collaborate and work closely with cross functional teams.
  • To meet the management expectations w.R.T timelines and quality.

To work closely within the team and provide training to new members on new regulatory requirements for Complex products.


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