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Eugia Pharma Hiring Regulatory Affairs Professionals | B.Pharm / M.Pharm | 2–8 Years
Eugia Pharma Research Centre is inviting applications from experienced professionals for Regulatory Affairs roles across US and Canada markets. This is a great opportunity to work with a leading pharmaceutical organization and grow your career in regulatory compliance and submissions.
Contents
🔹 Job Overview
- Company: Eugia Pharma
- Department: Regulatory Affairs (CMC & Labeling / Canada Market)
- Qualification: B.Pharm / M.Pharm
- Experience: 2 to 8 Years
- Location: Hyderabad
🔹 Open Positions
1. Regulatory Affairs – CMC & Labeling (US Market)
- Experience: 3–8 Years
- Key Responsibilities:
- Planning, reviewing, and submission of ANDA & NDA projects
- Drafting responses for FDA deficiencies with high-quality standards
- Handling submissions like CBE, CBE-30, PAS & Annual Reports
- Hands-on experience in labeling activities
2. Regulatory Affairs – Canada Market
- Experience: 2–4 Years
- Key Responsibilities:
- Dossier compilation for Injectable & OSD dosage forms
- Knowledge of ICH guidelines and regulatory procedures
- Lifecycle management (LCM) and supplement strategies
- Review of technical documents (Protocols, API, Drug Product)
- Preparation of regulatory submission documents
- Responding to agency queries within timelines
🔹 Required Skills
- Strong knowledge of global regulatory guidelines (USFDA/ICH/Canada)
- Experience in dossier preparation and submission
- Good documentation and communication skills
- Ability to manage regulatory timelines and compliance
📩 How to Apply?
Interested candidates can share their updated CVs to:
👉 reshma.thota@eugiapharma.com
📍 Work Location
Hyderabad (Pashamylaram, Patancheru)
Important Note
Eugia Pharma does not charge any fee for recruitment. Any communication asking for money should be considered fraudulent.
