Senior Global Regulatory Specialist - Medical Devices & IVD

Posted yesterday

selectekSan Jose (CA)

Regulatory Affairs Specialists Electromedical and Electrotherapeutic Apparatus Manufacturing

SENIORITY

Senior

Apply

About the role

Selectek, Inc. is seeking an experienced Senior Regulatory Affairs Specialist to lead global regulatory activities for its diagnostics, life sciences, and laboratory solutions portfolio. You will develop regulatory strategies, prepare submissions, and ensure ongoing compliance across markets. You will partner with cross-functional teams throughout the product lifecycle. Ideal candidates have at least 3 years in regulatory affairs within medical devices or IVD, experience with international

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.