About this opportunity
Selectek, Inc. lists this Global Regulatory Affairs Specialist for Med Devices & IVD opportunity in santa clara, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Selectek, Inc. is seeking an experienced Senior Regulatory Affairs Specialist to support 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. Responsibilities include coordinating with international teams, maintaining technical files, post‑market surveillance, and driving continuous improvement of regulatory processes across the product
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Worksite address
santa clara, CA, 95053, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.