Exalta Group is seeking a Regulatory Specialist 2 to lead regulatory strategy and global submissions for medical devices. The role requires interfacing with product development, quality, and manufacturing teams to ensure compliance across labeling, promotions, and documentation in line with global regulations.
You will influence regulatory decisions and support business objectives. The candidate will author and submit regulatory applications for MDSAP markets, EU, and UK, and help maintain
#J-18808-LjbffrRemote Global Regulatory Devices in workfromhome at Unknown Company
This position is listed as full time and onsite.