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Director, Regulatory Affairs

Posted today

veeva systemsSpringfield (IL)

SENIORITY

Manager

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About the role

Veeva Systems, Inc. is seeking an experienced MedTech Regulatory Information Management consultant to lead implementations worldwide. You will guide Regulatory Affairs and Operations transformations, working with Professional Services to deliver end-to-end data and documentation workstreams. The role emphasizes cross-team collaboration, customer liaison, and building adoption roadmaps while applying industry standards such as FDA, EU MDR/IVDR, and UDI.

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

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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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