Company Description ZimVie is a global life sciences company focused on dental implants, biomaterials, and digital dentistry solutions that support tooth replacement and restoration procedures. The organization offers a comprehensive portfolio, including dental implant systems, digital solutions, advanced workflows, and biomaterials designed to simplify procedures and enhance clinical outcomes. Headquartered in Palm Beach Gardens, Florida, with operations worldwide, ZimVie is dedicated to improving smiles, function, and confidence in daily life. As a recognized leader in its field, the company is committed to advancing clinical science and technology that underpin effective and reliable tooth replacement solutions.
Regulatory Affairs & Quality Assurance Specialist - APAC
We are looking for a detail-oriented and proactive Regulatory Affairs & Quality Assurance Specialist to support medical device product registrations across India and other APAC markets. This role will be responsible for managing regulatory submissions,
maintaining regulatory databases and quality management documentation, and supporting compliance with applicable medical device regulations and standards.
The ideal candidate will have experience in medical device regulatory affairs and quality systems, solid attention to detail, and the ability to work effectively with cross-functional and international teams.
Key Responsibilities
Manage medical device product registrations in India, including initial registrations, post-approval activities, amendments, and renewals.
Support and manage product registration activities across other APAC markets.
Maintain and update internal regulatory databases and ensure regulatory information is accurate and current.
Prepare, review, approve, distribute, and support training related to Quality Management System (QMS) documentation.
Participate in and support internal and external audits.
Provide training and guidance to relevant departments on quality and regulato
📌 QA&RA Specialist (Mumbai)
🏢 ZimVie
📍 Mumbai