Aliyan Pharma is inviting applications for the position of Regulatory Affairs Executive at its Iskon, Ahmedabad office. This is an excellent opportunity for experienced B.Pharm and M.Pharm professionals looking to build a rewarding career in Regulatory Affairs within the pharmaceutical industry.
Candidates with a minimum of 2 years of hands-on Regulatory Affairs experience in dossier preparation, CTD/ACTD documentation, and international product registrations are encouraged to apply. Immediate joiners or professionals who can join within 15 days will be given preference.
If you’re searching for Regulatory Affairs Executive Jobs in Ahmedabad, Pharma Regulatory Affairs Jobs 2026, or B.Pharm M.Pharm Regulatory Jobs, this opportunity could be your next career move.
Job Details
| Particular | Details |
|---|---|
| Company | Aliyan Pharma |
| Position | Regulatory Affairs Executive |
| Department | Regulatory Affairs |
| Location | Iskon, Ahmedabad, Gujarat |
| Qualification | B.Pharm / M.Pharm |
| Experience | Minimum 2+ Years |
| Employment Type | Full-Time |
| Preferred Joining | Immediate or Within 15 Days |
Key Responsibilities
The selected candidate will be responsible for:
- Preparing and submitting regulatory dossiers and product registration documents.
- Managing product registrations, renewals, variations, and regulatory submissions.
- Reviewing CTD, ACTD dossiers, Certificates of Analysis (COAs), stability reports, and technical documentation.
- Coordinating with manufacturers, customers, and internal departments for regulatory requirements.
- Responding to regulatory authority queries effectively.
- Maintaining regulatory databases, trackers, and documentation records.
- Supporting Business Development and Export teams by providing regulatory documentation.
- Ensuring compliance with pharmaceutical regulatory guidelines and documentation standards.
Eligibility Criteria
Applicants should possess:
- B.Pharm or M.Pharm qualification.
- Minimum 2 years of relevant Regulatory Affairs experience.
- Strong knowledge of:
- CTD & ACTD Dossier Preparation
- International Product Registrations
- Pharmaceutical Regulatory Compliance
- Regulatory Documentation
- Good communication and coordination skills.
- Excellent documentation abilities.
- Proficiency in Microsoft Office.
- Ability to manage multiple regulatory projects within timelines.
Important: Freshers are not eligible for this position.
Preferred Candidate Profile
Aliyan Pharma is looking for professionals who:
- Have practical Regulatory Affairs experience.
- Can work independently on dossier preparation and submissions.
- Have exposure to export regulatory documentation.
- Can join immediately or within 15 days.
Why Join Aliyan Pharma?
- Excellent opportunity in the Regulatory Affairs domain.
- Exposure to international pharmaceutical registrations.
- Professional growth in documentation and compliance.
- Collaborative work environment.
- Opportunity to work with Business Development and Export teams.
- Stable full-time pharmaceutical career in Ahmedabad.
How to Apply
Interested candidates meeting the eligibility criteria can:
📧 Email Resume: hr@aliyanpharma.com