Global Regulatory Affairs Lead, Medical Devices
envistaMahwah (NJ)
About the role
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.
Before you apply
Applying takes about a minute. These four things decide how fast it moves after that.
Your profile is current
It's what we read first. Occupations, seniority and locations matter more than a long history.
Two examples you can talk through
Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.
A number in mind
What you're on now and what would make you move. We negotiate better when we know both.
Your notice period
Employers plan around it, and it's the question that stalls offers most often.
Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.
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