The pharmaceutical industry continues to expand rapidly, creating strong demand for skilled professionals in Drug Regulatory Affairs (DRA). A leading pharma organization is currently hiring a DRA Executive in Noida for candidates with 2โ4 years of hands-on experience in regulatory documentation, dossier preparation, and compliance.
This role is ideal for candidates looking to grow in pharma regulatory affairs jobs in India, especially those experienced in CTD/ACTD submissions and regulatory coordination.
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Key Responsibilities โ DRA Executive
- Preparation and submission of CTD/ACTD dossiers for regulatory approvals
- Ensuring compliance with CDSCO, FSSAI, and AYUSH guidelines
- Coordination with internal departments like QA, QC, and R&D
- Managing regulatory documentation and lifecycle updates
- Tracking approval timelines and responding to regulatory queries
- Maintaining accurate records for audits and inspections
Required Qualifications & Skills
- Bachelorโs or Masterโs degree in Pharmacy, Life Sciences, or related field
- 2โ4 years of experience in Drug Regulatory Affairs
- Strong knowledge of regulatory submissions (CTD/ACTD)
- Familiarity with Indian regulatory authorities (CDSCO, FSSAI, AYUSH)
- Excellent documentation and communication skills
- Analytical thinking and attention to detail
Preferred Candidate Profile
- Experience in handling global regulatory submissions is a plus
- Ability to manage multiple projects simultaneously
- Strong understanding of pharma compliance frameworks
Salary & Benefits
- Salary Range: โน3.5 LPA โ โน6.5 LPA (based on experience)
- Opportunity to work in a fast-growing pharma regulatory environment
- Exposure to multiple regulatory markets and frameworks
- Career growth in Regulatory Affairs Pharma Jobs
Job Location
- Noida, Uttar Pradesh, India
How to Apply
Interested candidates can share their updated CV at: