BioMatrix Healthcare Pvt. Ltd., established in 2007 and headquartered in Ahmedabad, is a research-driven pharmaceutical company known for manufacturing oral solids, liquids, and dry syrup formulations.
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With approvals from WHO-GMP, EU-GMP, USFDA, Health Canada, and MHRA, and exports to 40+ countries, the company offers unmatched exposure to global regulatory frameworks and international markets.
💼 Job Role: International Regulatory Affairs (IRA)
Key Responsibilities
- Prepare and compile regulatory dossiers for ROW and semi-regulated markets
- Handle submissions across Asia, LATAM, CIS, Africa, GCC, and Europe
- Work on CTD, ACTD, and eCTD formats
- Manage product lifecycle: renewals, variations, query responses
- Ensure regulatory compliance and document accuracy
- Coordinate with internal teams for submission readiness
These responsibilities are critical in ensuring global drug approvals and compliance with international standards.
🎓 Eligibility & Qualifications
Education
- B.Pharm
- M.Pharm
- M.Sc
Relevant Specializations
- Regulatory Affairs
- Pharmaceutics
- Pharmaceutical Analysis
- Clinical Research
- Quality Assurance
Experience
- 1 to 10 years in regulatory affairs or related domain
Required Skills
- Dossier preparation & submissions
- CTD / eCTD expertise
- Knowledge of USFDA, EU, MHRA regulations
- Strong documentation & communication skills
- Exposure to global markets (preferred)
📍 Job Location & Salary
- Location: Ahmedabad (Corporate Office)
- Salary: ₹3.5 LPA – ₹12 LPA (based on experience)
- High growth potential in regulatory affairs careers
🚀 Walk-in Interview Details
- Date: 10 May 2026 (Sunday)
- Time: 09:30 AM – 01:00 PM
Venue:
BioMatrix Healthcare Pvt. Ltd.
Corporate Office, 502-B, Times Square Grand
Sindhu Bhavan Road, Thaltej
Ahmedabad – 380059
📧 Email Application
Candidates who cannot attend the walk-in can apply via email:
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