The pharmaceutical industry continues to expand its global footprint, and regulatory professionals are in high demand. Alde Medi Impex Limited is currently hiring a Drug Regulatory Affairs (DRA) Executive in Delhi, offering an excellent opportunity for candidates with experience in international regulatory affairs, dossier preparation, and CTD/eCTD submissions.
This role is ideal for professionals looking to strengthen their career in pharma regulatory affairs jobs in India, especially those with hands-on exposure to formulation dossiers and global regulatory compliance.
Job Details
- Position: DRA Executive (Drug Regulatory Affairs)
- Location: Delhi, India
- Experience Required: Minimum 2 Years
- Qualification: B.Pharm / M.Pharm
- Industry: Pharmaceutical / Regulatory Affairs
Key Responsibilities โ Regulatory Affairs Executive
As a Drug Regulatory Affairs Executive, you will be responsible for:
- Preparation, review, and submission of regulatory dossiers
- Compilation and filing of eCTD, CTD, and ACTD dossiers
- Managing country-specific regulatory submissions
- Handling product registrations in regulated and semi-regulated markets
- Ensuring compliance with global regulatory guidelines
- Maintaining accuracy in raw data documentation and validation
- Supporting international regulatory submissions and approvals
This role requires strong expertise in pharmaceutical regulatory documentation and compliance management.
Eligibility Criteria & Skills Required
Candidates applying for this DRA Executive job in Delhi must meet the following criteria:
- Educational Qualification: B.Pharm or M.Pharm
- Experience: Minimum 2 years in Regulatory Affairs or QC (Pharma Industry)
- Strong knowledge of Analytical Method Validation
- Hands-on experience with international regulatory submissions
- Familiarity with dossier lifecycle management (CTD/eCTD/ACTD)
- High attention to detail and documentation accuracy
Salary & Benefits
- Estimated Salary Range: โน3.5 LPA โ โน6 LPA (based on experience and expertise)
- Opportunity to work on global regulatory submissions
- Exposure to international pharmaceutical markets
- Career growth in regulatory affairs domain
- Collaborative and compliance-driven work environment
Why Join Alde Medi Impex Limited?
Joining Alde Medi Impex Limited means becoming part of a growing pharmaceutical company focused on regulatory excellence and global expansion. Professionals will gain valuable exposure to international regulatory frameworks, dossier submissions, and product registrations, making it a strong career-building opportunity in drug regulatory affairs.
How to Apply
Interested candidates can apply using the following details:
- Email: hrops@aldemedi.com
- Phone: 9289857466
Ensure your CV highlights your experience in regulatory affairs, CTD/eCTD submissions, and international dossier handling.