Base Medico Pvt. Ltd. is hiring Regulatory Affairs Professionals for its Vadodara (Gujarat) location. If you are a B.Pharm or M.Pharm graduate with 1–3 years of hands-on RA experience, this is a great opportunity to grow your career in the global pharmaceutical regulatory domain.
📝 About the Role – Regulatory Affairs
As a Regulatory Affairs professional, you will be responsible for preparing and submitting regulatory dossiers for Africa, LATAM, and ASEAN markets, ensuring compliance with international regulatory requirements, and supporting business expansion activities.
📌 Key Responsibilities
- Preparation and compilation of CTD / ACTD dossiers
- Handling regulatory submissions for Africa, LATAM & ASEAN regions
- Ensuring compliance with country-specific regulatory guidelines
- Coordination with cross-functional teams (QA, R&D, Production)
- Supporting product registrations and lifecycle management activities
📚 Eligibility & Requirements
- 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 deadline-driven approach
🌈 What Base Medico Offers
- Opportunity to work with a growing pharmaceutical company
- Competitive salary and benefits package
- Exposure to global regulatory markets
- Professional learning and career growth
- Supportive and collaborative work culture
📍 Job Location
Vadodara, Gujarat – India
📧 How to Apply
Interested candidates can apply by:
- 📩 Emailing CV to hr@basemedico.com
- 📲 WhatsApp / Call: 92743 95085
Book
🌐 About the Company
Base Medico Pvt. Ltd. is a reputed pharmaceutical organization focused on delivering high-quality products while maintaining strict regulatory compliance across global markets.
🚀 Don’t miss this opportunity!
If you’re looking to build a strong career in Regulatory Affairs, apply now and take the next step toward global pharma exposure.
