The pharmaceutical industry is one of the most strictly regulated sectors in the world. Behind every life-saving drug on the pharmacy shelf lies a mountain of legal documentation, compliance checks, and government approvals.
Noronic Pharmaceutical Pvt. Ltd., a rising name in the pharma landscape, is currently hiring a Regulatory Affairs (RA) Officer – Legal for their office in Gota, Ahmedabad. 💊✨
If you’re detail-oriented and confident in handling pharmaceutical legal documentation and government liaisoning, this could be your next big career move.
🔍 Understanding the Role: RA Officer (Legal)
In pharmaceutical companies, the Regulatory Affairs department acts as the bridge between products and government health authorities.
At Noronic Pharmaceutical, the Legal-focused RA role means you will:
- Be the custodian of company licenses and permissions
- Ensure documentation aligns with the Drugs and Cosmetics Act and related legal frameworks
- Secure approvals that allow products to reach the market
This position is ideal for professionals who enjoy structured documentation, legal compliance, and interacting with regulatory bodies.
📋 Key Responsibilities & Core Duties
1️⃣ Licensing & Permissions 📜
You will manage and submit applications for:
- Product Permission
- COPP (Certificate of Pharmaceutical Product)
- FSC (Free Sale Certificate)
- Product Registration & Lifecycle Management
These certifications are essential for both domestic and international pharmaceutical trade.
2️⃣ Legal Documentation & Review ⚖️
Accuracy is critical. Your responsibilities will include:
- Drafting Undertakings and Declarations
- Preparing and reviewing Agreements with third parties
- Ensuring compliance with the latest amendments in pharma laws
- Verifying documentation before submission to authorities
3️⃣ Regulatory Compliance 🛡️
- Acting as an internal compliance checkpoint
- Minimizing regulatory queries and rejections
- Ensuring 100% adherence to current legal standards
4️⃣ Authority Liaising & Follow-Ups 🤝
You will coordinate with regulatory authorities regarding:
- New product approvals
- License renewals
- Compliance clarifications
- Ongoing regulatory matters
Persistence and professional communication are key here.
✅ Who Should Apply? (Candidate Profile)
Noronic Pharmaceutical is looking for:
- Experience: 1–2 years in Regulatory Affairs or Pharma-Legal roles
- Gender Preference: Female candidates 👩💼
- Location: Candidates residing in or willing to commute to Gota, Ahmedabad
- Core Skills:
- Strong documentation skills
- Familiarity with COPP & FSC processes
- Excellent follow-up and coordination abilities
- Attention to legal detail
⏰ Work-Life Balance
- Working Hours: 09:30 AM – 06:00 PM
- Structured corporate schedule
- No irregular shift burden
A stable timing structure allows professional growth without burnout.
📩 How to Apply (Step-by-Step Guide)
📧 Email: hr@noronicpharma.com
✔ Application Checklist:
- Update your CV with:
- COPP & FSC handling experience
- Product Permission submissions
- License renewals handled
- Highlight successful regulatory approvals
- Mention authority coordination experience
📌 Suggested Subject Line:
Application for RA Officer (Legal) – [Your Name] – [1-2 Years Experience]
🌟 Why Ahmedabad?
Ahmedabad, especially Gujarat, is considered one of India’s largest pharmaceutical hubs. The state contributes significantly to India’s pharmaceutical manufacturing and exports.
Working in Gota places you right inside a strong pharma ecosystem with long-term career growth potential. 📈
