Base Medico Pvt. Ltd. is hiring experienced Regulatory Affairs Professionals in Vadodara, Gujarat. This is an excellent opportunity for B.Pharm / M.Pharm graduates with hands-on regulatory exposure who are looking to grow their career in the pharmaceutical industry.
🧪 About the Role – Regulatory Affairs
As a Regulatory Affairs professional, you will be responsible for CTD/ACTD dossier preparation and submissions across Africa, LATAM, and ASEAN markets. You will work closely with cross-functional teams to ensure regulatory compliance and timely approvals.
📌 Key Responsibilities
- Preparation and submission of CTD / ACTD dossiers
- Handling regulatory submissions for Africa, LATAM, and ASEAN regions
- Ensuring compliance with country-specific regulatory requirements
- Coordination with internal teams for documentation and query responses
- Supporting regulatory strategies for business growth
🎓 Eligibility Criteria
- Experience: 1–3 years in Regulatory Affairs
- Qualification: B.Pharm / M.Pharm
- Hands-on experience in CTD / ACTD dossier preparation
- Strong understanding of international regulatory requirements
- Detail-oriented, proactive, and organized approach
🌟 Why Join Base Medico Pvt. Ltd.?
- Work with a growing pharmaceutical company
- Competitive salary with benefits
- Exposure to multiple international markets
- Professional learning and long-term career growth
- Supportive and collaborative work environment
📧 How to Apply
Interested candidates can apply through the following channels:
- 📩 Email: hr@basemedico.com
- 📱 WhatsApp / Call: 92743 95085
📌 Mention “Regulatory Affairs – Vadodara” in the subject line while applying.
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🏢 About the Company
Base Medico Pvt. Ltd. is a reputed pharmaceutical organization committed to delivering high-quality healthcare products while maintaining global regulatory standards.
