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Drug Regulatory Affairs Jobs at Florencia Healthcare

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If you’re seeking Drug Regulatory Affairs jobs in Noida with a reputed pharmaceutical company, this opportunity at Florencia Healthcare could be a strong career move. The company is actively hiring skilled professionals for its Regulatory Affairs team, focusing on candidates with hands-on experience in CTD and ACTD submissions.

With increasing demand for compliance-driven pharmaceutical operations, Regulatory Affairs professionals in India are becoming critical assets. This role offers exposure to regulatory frameworks, dossier preparation, and global submission standards.


Job Overview

  • Position: Drug Regulatory Affairs (DRA)
  • Location: Delhi NCR / Noida
  • Experience: 1โ€“5 Years
  • Qualification: B.Pharm / M.Pharm
  • Job Type: Full-Time
  • Joining: Immediate

Key Responsibilities โ€“ Drug Regulatory Affairs Role

  • Preparation and compilation of CTD (Common Technical Document) and ACTD dossiers
  • Managing regulatory submissions for domestic and international markets
  • Ensuring compliance with CDSCO and global regulatory guidelines
  • Coordination with cross-functional teams (QA, QC, R&D)
  • Tracking and responding to regulatory queries and deficiencies
  • Maintaining updated knowledge of pharmaceutical regulatory requirements

Required Qualifications & Skills

  • Bachelorโ€™s or Masterโ€™s degree in Pharmacy (B.Pharm / M.Pharm)
  • 1โ€“5 years of experience in Drug Regulatory Affairs
  • Strong understanding of CTD, ACTD, and dossier preparation
  • Familiarity with regulatory guidelines (CDSCO, ICH)
  • Good documentation and communication skills
  • Ability to work under deadlines in a regulatory environment

Why Choose a Career in Regulatory Affairs?

The demand for Regulatory Affairs jobs in India is rapidly growing due to stricter compliance norms and global pharmaceutical expansion. Professionals in this field gain:

  • High career stability in pharma industry
  • Opportunities to work on international regulatory submissions
  • Exposure to evolving drug approval processes
  • Competitive salary growth and specialization paths

Salary & Benefits

  • Estimated Salary: โ‚น3.5 LPA โ€“ โ‚น7.5 LPA (based on experience)
  • Professional growth in a reputed pharma organization
  • Hands-on experience in global regulatory documentation
  • Collaborative and growth-oriented work environment

How to Apply

Interested candidates can apply or refer suitable profiles:

Tip: Mention โ€œApplication for Drug Regulatory Affairs โ€“ Immediate Joinerโ€ in your email subject for better visibility.

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