Overview

Mave is building a neurotechnology wearable designed for everyday use. Backed by 25+ years of foundaxtional neuroscience learnings and paired with expert support, we’re creating a new kind of product for everyday mental health- one that actually helps people feel better (anxiety, low mood, burnout, etc).

We're early — the kind of early where your decisions will shape the product, the team, and the category. It’s the dawn of neuroscience as a consumer technology, and you’ll be right at the heart of it.

Location: Bangalore (in-office from Koramangala)

Type: Full-time

Experience: 2+ years in QA/RA

What You’ll Do

• Assist in the end-to-end implementation of QMS as per ISO 13485 and 21 CFR part 820 requirements
• Work on existing regulatory projects by aiding in the creation of regulatory documents
• Work closely with cross-functional departments such as the Engineering team to support the implementation of Design Control and Risk Management activities
• Conduct training of cross-functional teams on the QMS processes
• Manage the QMS activities such as Change Control, Risk Management, Post Market activities, NCRs, CAPAs, Complaints etc

Must Have

• Minimum 2 years of work experience
• Knowledge about standards such as ISO 13485, ISO 14971, IEC 62304, and IEC 62366 is preferred
• Ability to interpret and analyze the regulatory standards and guidelines
• Good writing skills in accordance with good documentation practices