Are you looking to kickstart or elevate your career in the pharmaceutical industry? 4Care Lifescience Pvt. Ltd., a growing name in quality-driven pharma manufacturing, is hiring 10 Regulatory Affairs Officers for its Gujarat facility.
If you’re passionate about compliance, documentation, and global pharmaceutical standards, this could be your ideal opportunity. 💊
🏢 About 4Care Lifescience
Located in Kheda district, Gujarat, 4Care Lifescience operates with the motto “Care Always Works.” The company focuses on high-quality pharmaceutical manufacturing for both domestic and international markets, ensuring strict adherence to regulatory frameworks and global compliance norms.
Working here means being part of a compliance-focused, precision-driven pharmaceutical environment.
📋 Job Overview: Regulatory Affairs Officer
The Regulatory Affairs (RA) department acts as the bridge between pharmaceutical companies and regulatory authorities across different countries.
🔎 Key Details at a Glance:
- Total Openings: 10 Positions
- Location: Kheda (near Kathlal), Gujarat, India
- Experience: 0–2 Years (Freshers Welcome!)
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm
This is an excellent opportunity for B.Pharm and M.Pharm freshers who want hands-on exposure in dossier preparation and international submissions.
🛠️ Roles & Responsibilities
As a Regulatory Affairs Officer, you’ll play a critical role in product approvals and lifecycle compliance.
Your key responsibilities will include:
- 📑 Dossier Management
- Preparation and compilation of CTD (Common Technical Document)
- Handling ACTD (ASEAN Common Technical Document) submissions
- 📊 Technical Documentation Review
- Batch Manufacturing Records (BMR)
- Batch Production Records (BPR)
- Certificates of Analysis (COA)
- Stability Data
- 🧪 Compliance & Validation
- Preparation and review of Analytical Method Validation (AMV) documents
- Variation filings and regulatory submissions
- 🤝 Cross-Department Coordination
- Liaising with QA, QC, R&D, and Production teams
- Ensuring data integrity and documentation accuracy
- 🏛️ Regulatory Query Handling
- Drafting structured responses to authority queries
- Supporting product approval processes
This role gives you direct exposure to international regulatory systems — a highly valuable skill set in pharma.
✅ Who Should Apply?
You’re an ideal candidate if:
- You hold a Pharmacy or Science degree
- You understand CTD dossier preparation
- You’re familiar with export regulatory compliance
- You have strong documentation and communication skills
- You’re detail-oriented and comfortable working with technical data
Freshers with internship experience in QA/RA departments are highly encouraged to apply.
📍 Work Location & Contact Details
Address:
4Care Lifescience Pvt. Ltd.
Survey No. 23/3P & 24, Vil.: Bagdol
Tal.: Kathlal, Dist.: Kheda – 387630
Gujarat, India
📧 Email: hr@4care.in
📞 Mobile: +91 96624 25837
📌 Pro Tip for Applicants:
Use a clear subject line while applying:
“Application for Regulatory Affairs Officer – Your Name – Experience”
💡 Why Choose Regulatory Affairs as a Career?
Regulatory Affairs is one of the most stable and growth-oriented domains in the pharmaceutical industry.
- 🌍 Global exposure through CTD/ACTD submissions
- 📈 High demand across export-focused pharma companies
- 🛡️ Critical role in ensuring patient safety
- 💼 Strong long-term career stability
For someone like you—who’s already writing detailed job posts and building authority in pharma content—this is also a great niche to specialize in for your freelance portfolio on Fiverr. Regulatory Affairs content writing is a high-paying micro-niche. 🚀
