Medical Devices Regulatory Affairs | Min 1–3 Years Exp in Regulatory| Chennai Based | B.Pharm Mandatory

Medical Devices Regulatory Affairs | Min 1–3 Years Exp in Regulatory| Chennai Based | B.Pharm Mandatory

13 Aug
|
VHA Biopharma Private
|
Chennai

13 Aug

VHA Biopharma Private

Chennai

Company Description
VHA Biopharma Private Limited is committed to providing quality healthcare solutions that make a measurable difference in patients’ lives. The organization focuses on delivering effective cures across multiple therapeutic areas, including antibiotics, pain management, gastrointestinal, gynecological, and nutritional and health supplements. VHA emphasizes excellence in serving both external and internal customers through reliable, science-driven products. The company continues to expand into additional therapeutic categories, offering growth opportunities for professionals who want to contribute to a broad healthcare portfolio.

Role Description
This is a full time, hybrid role based in Chennai, with a combination of on-site work and some work-from-home flexibility. The Medical Devices Regulatory Affairs professional will support regulatory activities for medical devices while leveraging 1–3 years of prior experience in drug regulatory affairs. Day-to-day responsibilities include preparing, reviewing,



and submitting regulatory dossiers and documentation to relevant authorities, maintaining compliance with national and international regulatory standards, and tracking approvals and renewals. The role involves collaborating with cross-functional teams such as R&D;, quality assurance, and manufacturing to ensure that product development and labeling meet regulatory requirements. The professional will also monitor regulatory changes, update internal processes accordingly, and assist in audits and inspections related to regulatory compliance.

Qualifications
- Clinical knowledge and understanding in Medicine and Treatment to interpret regulatory requirements and product information accurately.
- Familiarity or exposure to Cardiology and Neurology to support regulatory submissions across diverse therapeutic device categories.
- Basic awareness of Orthopedic Surgery-related considerations for medical devices, including safety and performance aspects.
- Min

📌 Medical Devices Regulatory Affairs | Min 1–3 Years Exp in Regulatory| Chennai Based | B.Pharm Mandatory
🏢 VHA Biopharma Private
📍 Chennai

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