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

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Level

Senior

Location

San Jose, CA

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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