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Company: Aarti Pharmalabs
Location: Nerul, Navi Mumbai, Maharashtra
Positions Available: 5
Qualification: MSc or Ph.D. in Chemistry
Experience Required: 2-10 Years

Key Responsibilities:

  • Submit DMF (Drug Master Files) and manage eCTD (electronic Common Technical Document) submissions.
  • Provide technical advice for regulatory documents.
  • Manage and review documents, including Letters of Authorization (LOA) and Certificates of Suitability (CEP).
  • Handle change controls and submit annual reports and amendments.
  • Respond to queries from customers and regulatory authorities.
  • Coordinate with various departments for DMF submissions.

Eligibility Criteria:

  • Experience in DMF filing and eCTD publishing.
  • Experience in managing a team.

How to Apply:

Application Link

Aarti Pharmalabs Hiring Regulatory Affairs Executive / Sr. Executive / Dy Manager