Novumgen
2-4years
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🚀 Executive – Regulatory & Scientific Affairs (Formulations) | Vadodara
Novumgen is looking for a regulatory professional with 2–4 years of experience to support pharmaceutical formulation products and regulatory activities for European & UK markets.
🔹 Location: Vadodara
🔹 Experience: 2–4 Years
🔹 Department: Regulatory & Scientific Affairs – Formulations
🔬 Key Responsibilities
* Prepare and review CMC documentation for pharmaceutical formulation products
* Compile and maintain CTD/eCTD dossiers for registrations, variations, renewals and post-approval submissions
* Support regulatory submissions and responses to Health Authority queries
* Ensure dossiers comply with applicable European and UK regulatory requirements
* Coordinate with regulatory authorities and cross-functional teams throughout the product lifecycle
* Identify regulatory risks and ensure timely compliance with evolving global requirements
🎓 Qualification
* B.Pharm / M.Pharm
* Life Sciences / relevant pharmaceutical qualification with applicable regulatory experience
🎓 Qualification
* B.Pharm / M.Pharm
* Life Sciences / relevant pharmaceutical qualification with applicable regulatory experience
💡 Ideal Candidate
Professionals with hands-on experience in CMC documentation, CTD/eCTD preparation, regulatory submissions and lifecycle management, along with strong documentation and communication skills.
FYND Talent Solutions is an independent recruitment platform. This job is shared for informational purposes only and is not an official communication from the hiring company unless explicitly stated.
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MailTo apply for this job email your details to raghulr190300@gmail.com