Versah, LLC, now part of the Envista family, seeks a Regulatory Affairs leader to develop global strategies and maintain regulatory approvals for its medical device portfolio. You will collaborate with R&D, Engineering, Quality, Operations, Marketing, and Sales to support product lifecycle activities.
The role emphasizes compliance with 21 CFR 820, ISO 13485, and EU MDR, while guiding audits and regulatory interactions across markets.
#J-18808-LjbffrGlobal Regulatory Affairs Lead, Medical Devices in mahwah at Unknown Company
This position is listed as full time and onsite.