Senior QA Associate, Medical Device Compliance

Alcon in Malaysia seeks a Regulatory Reports & Complaint Handling professional to manage day-to-day regulatory submissions for medical devices and oversee complaint records across products. You will ensure timely reporting, data accuracy, and adherence to local and international regulations.

The role requires at least 2 years in pharma/medical devices, strong writing and cross-functional collaboration, and the ability to work across time zones.