Regulatory Affairs Intern – Medical Devices

Work directly with the founder on FDA submissions for medical devices. You will research regulatory pathways, review test data, help draft parts of submissions and join client calls. The role also includes some business development, such as speaking with clients and building relationships.

Who Should Apply • Past hands-on work with medical devices (job or internship) in regulatory, testing, quality or R&D; • Well spoken in English, outspoken and confident with current people • Eager to learn and open to feedback • Degree in Life Sciences, Biomedical Engineering, Biotechnology, Bachelors or Engineering

What You Will Gain • Learn how medical devices get approved by the U.S. FDA, from a former FDA reviewer • Hands-on submission work and real client exposure • The chance to learn every part of the regulatory work if you want to, from research and testing to FDA submissions • Business development experience alongside regulatory work A full-time role based on performance, with room to grow as the company expands Details 6-month internship | Office in Balewadi, Pune

How to Apply Email your CV to: [email protected]

Subject: Application – Regulatory Affairs Intern

📌 Regulatory Affairs Intern – Medical Devices (Pune)
🏢 Tacticity Advisors
📍 Pune