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Deputy Manager, Regulatory Affairs

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  • 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.

  • Suitably qualified individuals with strong Scientific and Regulatory background.
  • Academic degree in Pharmacy (M. Pharm or PhD), with preferably specialization in Regulatory Affairs or Pharmaceutics.
  • Experienced (minimum 8-10 years) in Regulatory Affairs with Injectable dosage form and overall experience 12+ years.
  • End to end complete understanding of Complex Products for US/ EU market right from Strategy, Filing, Deficiency response etc.
  • Experienced in drafting controlled correspondences, Meeting packages etc.
  • Experience being an active contributor to cross-functional teams and/or working in matrix organizations. High quality, critical thinking, process, and performance orientated; prioritizes activities and projects.
  • Exercises good judgment on regulatory, quality, and technical related compliance issues. High personal integrity; trustworthy; strong compliance and quality mind-set.
  • Solution orientated, strong sense of ownership and accountability.
  • Collaborative, team-oriented approach, capable of working cross-functionally, and in a matrixed and integrated way.

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