Are you a detail-oriented pharmaceutical professional ready to level up your career in Gujarat’s fast-growing pharma hub? If precision, compliance, and the art of drug documentation excite you—this one’s for you.
Pharmlite Pharmaceutical is expanding and inviting a skilled Regulatory Affairs Executive to join our dynamic team in Vadodara. If ensuring that life-saving medicines meet the highest safety and legal standards is your calling, we’d love to connect. 🩺✨
🔍 Understanding the Role: What is Regulatory Affairs?
In pharma, Regulatory Affairs (RA) is the critical bridge between innovation and patients. The RA team works closely with global and domestic authorities (FDA, EMA, CDSCO) to ensure products are developed, manufactured, and marketed in full compliance.
You’re not “just filing papers”—you’re the guardian of compliance, enabling medicines to reach the people who need them most. 💊
📝 Key Responsibilities & Expectations
Here’s what your day-to-day impact will look like:
- Dossier Mastery: Prepare, compile, and review regulatory dossiers (CTD/eCTD) with absolute accuracy. 📂
- Product Registrations: Manage the full lifecycle—submissions, renewals, variations.
- Strategic Coordination: Act as the liaison between R&D, QC, Manufacturing, and regulatory bodies. Clear communication is key. 🗣️
- Compliance Surveillance: Track and interpret regulatory updates to keep processes aligned and future-ready. ⚖️
🎓 Who Are We Looking For?
- Education: B.Pharm or M.Pharm with a strong foundation in pharmaceutical sciences. 🎓
- Experience: 1–3 years of hands-on regulatory documentation experience (domestic and/or international).
- Local Talent: This role is strictly for Vadodara-based candidates. We value strong local roots and team stability. 📍
🌟 Why Choose Pharmlite Pharma?
- Career Growth: Exposure to domestic and international regulatory landscapes—build a globally relevant profile. 📈
- Supportive Culture: Mentors, not micromanagers. Collaboration comes first. 🤝
- Innovation-Driven: Proactive ideas and process improvements are encouraged and rewarded.
📍 Life in Vadodara: The Pharma Capital
Vadodara blends rich culture with modern industrial momentum and is quickly becoming a powerhouse for pharmaceutical manufacturing and compliance excellence. For RA professionals, it’s the center of action—surrounded by leaders, facilities, and opportunity. 🏛️🏢
📧 How to Apply
Vadodara candidates only, please share your updated CV via:
- LinkedIn Message: Reach out to our hiring team
- Email: info@pharmlitepharma.com 📩
Subject Line (Recommended):
Application for Regulatory Affairs Executive – [Your Name] – [Years of Experience]
💡 Final Tips for Applicants
Regulatory Affairs values consistency and integrity. Make sure your CV highlights:
- Types of submissions handled (CTD/eCTD, DCP, MRP, etc.)
- Regions covered (India, EU, US, ROW) 🌍
- Your role in cross-functional coordination and compliance upkeep
Healthcare isn’t just a business—it’s a responsibility. Join our RA team and become part of the chain that delivers health and hope worldwide.
Apply today and help shape the future of healthcare. 🚀✨
