Regulatory Affairs – Medical Devices (Full time)
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.
Who Should Apply • Hands-on experience in medical device regulatory affairs is required. Work on an FDA submission (510(k), De Novo or PMA) is a plus. • Well spoken in English, outspoken and confident with new people • Eager to learn and open to feedback • Degree in Life Sciences, Biomedical Engineering, Biotechnology, Pharmacy 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 • Room to grow with the company as it expands
Details Full-time role | Office in Balewadi, Pune
How to Apply Email your CV to:
[email protected]
Subject: Application – Regulatory Affairs – Full-Time
📌 Regulatory Affairs – Medical Devices (Full-Time) (Pune)
🏢 Tacticity Advisors
📍 Pune