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Drug Regulatory Affairs Executive

--Punjab, Haryana, himachal Pradesh--

Location: Chandigarh / Baddi

Experience: Minimum 4 Years

Salary: ₹25,000+ (Based on experience)

Job Summary:

We are looking for an experienced Drug Regulatory Affairs Executive with strong expertise in preparing and submitting dossiers for export markets. The ideal candidate will have good exposure to regulatory frameworks and documentation processes required for pharmaceutical exports.

Key Responsibilities:

  • Prepare, compile, and submit drug dossiers for export approvals in compliance with international regulatory standards
  • Liaise with regulatory authorities and ensure timely approvals for export documentation
  • Maintain up-to-date knowledge of global regulatory requirements and ensure company compliance
  • Coordinate with production, quality, and R&D teams to gather necessary data for dossier preparation
  • Track and manage regulatory submissions, renewals, and registrations
  • Handle documentation related to import/export licenses, product registrations, and regulatory audits
  • Support internal teams with regulatory guidance and compliance requirements

Qualifications & Skills:

  • Bachelor’s degree in Pharmacy, Life Sciences, or related field
  • Minimum 4 years of experience in Drug Regulatory Affairs with focus on exports and dossier submission
  • Good understanding of global regulatory frameworks (e.g., USFDA, EMA, WHO, ICH guidelines)
  • Strong documentation and communication skills
  • Ability to work independently and manage multiple regulatory projects

Salary & Benefits:

  • ₹25,000+ per month, negotiable based on experience
  • Benefits as per company policies