Are you an experienced professional in regulatory publishing looking to elevate your career with a global biotechnology leader? Look no further. Regeneron, one of the most innovative biotech companies in the world, is actively hiring for the role of Regulatory Publishing Specialist at its Bengaluru office.
This is a golden opportunity for candidates with a life sciences background and 2+ years of regulatory publishing experience to join a dynamic and high-impact team working at the intersection of science and technology.
🧬 About Regeneron:
Regeneron is known for developing breakthrough medicines in areas like oncology, immunology, and genetics. The company’s workplace stands out for its innovation-driven culture, diverse workforce, and employee-first mindset. From its global headquarters to its India operations, Regeneron offers a blend of scientific excellence and career growth opportunities.
Whether you’re working on regulatory submissions or collaborating with international teams, you will always be part of something meaningful.
💼 Job Overview:
- 📌 Position: Regulatory Publishing Specialist
- 🏢 Company: Regeneron
- 📍 Location: Bengaluru, Karnataka
- 🪙 Salary: ₹8 LPA (Approx.)
- 📆 Experience Required: Minimum 2 years
- 🎓 Qualifications: B.Pharm, M.Pharm, M.Sc, Life Sciences, Regulatory Affairs, or Medical Devices
- 💼 Department: Global Development
- 🆔 Job Code: R38896
🔧 Key Responsibilities:
In this role, your work will directly support global regulatory submissions and compliance documentation. Here’s what you’ll be expected to handle:
- Format, compile, and publish electronic regulatory submissions such as INDs, CTAs, BLAs, MAAs, and JNDAs.
- Use publishing software like Lorenz Docubridge to validate and prepare documents for submission.
- Ensure compliance with FDA, EMA, ICH, and other regulatory standards.
- Archive and manage documents using Veeva Vault.
- Support in regulatory inspections and internal audits.
- Collaborate with vendors and internal teams for smooth document handling.
- Troubleshoot technical issues related to regulatory submissions.
- Assist in continuous improvement of regulatory systems and processes.
This role is technical, precise, and vital to the drug approval process. You’ll become an integral part of the global submission lifecycle.
🧠 Skills & Tools Required:
To be a strong fit for this role, you should possess:
- Minimum 2 years of hands-on experience in regulatory publishing.
- Excellent command of Microsoft Word and Adobe Acrobat for formatting complex documents.
- Knowledge of eCTD validation, XML tagging, and EDMS (Electronic Document Management Systems).
- Familiarity with Veeva Vault for archiving and lifecycle management.
- Proficiency in Lorenz Docubridge or similar regulatory publishing tools.
- Strong attention to detail, organizational, and communication skills.
If you’ve worked in regulatory submissions in the past and are comfortable managing large documentation projects, this role is a great match.
🌟 Why Choose Regeneron?
Here’s what makes Regeneron stand out from the crowd:
- 🌍 Global Biotech Leader: Contribute to life-changing drugs approved across the globe.
- 📈 Career Advancement: Clear growth paths and learning opportunities through international exposure.
- 💼 Cutting-Edge Work: Be a part of submission processes that influence FDA and EMA approvals.
- 🏥 Employee Benefits: Insurance, wellness programs, performance bonuses, and paid leave.
- 🤝 Inclusive Culture: Regeneron prides itself on its diverse and equal-opportunity workplace culture.
✅ Candidate Checklist Before Applying:
Here’s a quick checklist to know if you’re ready for this role:
| ✅ Requirement | 🔍 Status |
|---|---|
| B.Pharm / M.Pharm / M.Sc Degree | ✅ |
| 2+ Years of Regulatory Publishing | ✅ |
| Hands-on with Veeva, Adobe, Docubridge | ✅ |
| Familiarity with eCTD Standards | ✅ |
| Attention to detail & problem-solving | ✅ |
| Ready to work full-time from Bengaluru | ✅ |
If all of these are checked off—get your resume updated now!
🧭 Career Path After This Role:
Joining Regeneron as a Regulatory Publishing Specialist can open doors to senior roles such as:
- Regulatory Submissions Manager
- Regulatory Affairs Lead
- Document Control & Compliance Analyst
- Clinical Documentation Expert
The experience you’ll gain in global submission standards and document lifecycle management will be valued across the entire pharmaceutical industry.
💬 Final Thought:
If you’re passionate about contributing to global health solutions and enjoy working with detailed regulatory documentation, this role is tailor-made for you. Regeneron is not just hiring; they are building the future of biotech—one submission at a time.
Polish your resume, highlight your experience with publishing platforms, and prepare for a career leap.
📢 Bonus Tip:
In your resume or interview, don’t forget to mention:
- Specific regulatory agencies you’ve worked with (e.g., FDA/EMA)
- Tools you’ve used (especially Veeva Vault and Lorenz Docubridge)
- Any successful submissions or inspection readiness projects
Stay tuned to this blog for more verified pharmaceutical, life sciences, and healthcare job alerts!
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