Looking to advance your career in pharmaceutical regulatory affairs? Here’s a great opportunity!
Allotab Healthcare LLP is hiring skilled professionals for the position of Regulatory Affairs Specialist. If you have experience in global regulatory submissions and dossier management, this role is ideal for you.
Position Details
- Role: Regulatory Affairs Specialist
- Industry: Pharmaceutical
Key Responsibilities
- Preparation, compilation, and submission of CTD, eCTD, ACTD, and country-specific dossiers for international markets
- Review and approval of packaging artworks, labels, and product literature
- Handling responses to MOH queries, deficiency letters, and regulatory communications
- Maintenance of regulatory databases, product dossiers, and lifecycle documents
- Coordination with Manufacturing, R&D, QA, and QC teams for documentation and submissions
- Ensuring compliance with WHO-GMP, ICH Guidelines, EU-GMP, and global regulatory standards
Candidate Requirements
✔ Strong knowledge of international regulatory submissions
✔ Experience in pharmaceutical regulatory affairs
✔ Excellent documentation and communication skills
✔ Ability to manage multiple projects and timelines
✔ Strong coordination with cross-functional teams
Job Location
(To be confirmed by employer)
How to Apply
Interested candidates can share their updated resumes at:
📩 Email: info@allotabhealthcare.com
Why Join Allotab Healthcare?
✔ Opportunity to work on global regulatory submissions
✔ Exposure to international pharmaceutical markets
✔ Dynamic and growth-oriented work environment
✔ Career advancement in Regulatory Affairs domai
FAQs
Q1: What is the required experience?
Candidates with relevant regulatory affairs experience in pharma industry.
Q2: What types of dossiers are required?
CTD, eCTD, ACTD, and country-specific dossiers.
Q3: Is international exposure required?
Yes, experience in global regulatory submissions is preferred.
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