Looking for a talented and experienced Regulatory Affairs (Site RA) professional to join our team.
Robust knowledge of Regulatory requirements for Asia, Africa, or Europe markets.
Prepare and review regulatory dossiers for OSD products and ensuring compliance with global regulatory requirements (E.g , E.U, M.H.R.A)
Voordinate4 with varoius teams (R&D;, QA , QC) for data collection and dossier preparation.
Handlr regularory queries and having upto date knowledge of Regulatorty requirements.

B.Pharm & M.Pharm (RA) Qualification is required.

At RPG Life Sciences, we are driven by a singular purpose — delivering patient happiness through innovation and trust. We are committed to creating high-quality, affordable healthcare solutions that improve lives and strengthen the confidence of patients and healthcare partners alike.
We are proud to be a part of the renowned RPG Group, one of India’s most respected business conglomerates. Backed by the Group’s strong values of integrity, excellence, and long-term vision,



we carry forward a legacy that spans over four decades of nation-building and responsible growth.
Our journey is rooted in this legacy. We were created with the vision of building a focused, research-driven pharmaceutical business under the RPG umbrella—combining global-quality manufacturing, strong scientific capabilities, and deep market understanding. Over the years, we have evolved into a trusted name in key therapeutic areas such as cardiology, nephrology, gastroenterology, orthopedics, and anti-infectives.
We are powered by world-class manufacturing facilities and robust R&D; capabilities that meet stringent global standards. More importantly, we are built on trust — trust earned through consistency, quality, and ethical practices.
We are RPG Life Sciences — where legacy meets innovation, and every step we take is guided by our commitment to delivering better health and greater happiness.

📌 Sr Executive-Regulatory Affairs (Ankleshwar)
🏢 RPG Life Sciences
📍 Ankleshwar