Job Description:

  • Recruitment, Training and Developing Team
  • Building Competencies in the team to handle CMC Variations
  • Evaluating and Reporting team performance against Key Indicators.
  • Participating in Continuous process Improvement activities in assigned area
  • Understands regulations, guidelines, procedures, and policies relating to registration and manufacturing of pharmaceutical products/registration data management/submission format to expedite submission, review, and approval of global applications.
  • Team Management besides delivering Individually
  • Independently manage multiple projects and complexities

Qualification: B.Pharma/B.Sc or Equivalent Regulatory Experience

Experience: Minimum 10 Years in DRA, in CMC Variations or related

Salary: Negotiable

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