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Novo Nordisk

Fremont, California

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Newberg, Oregon

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Omeros Corporation

Seattle, Washington

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Olympus Corporation of the Americas

Massachusetts

Aadi Bioscience Inc

Nationwide

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Mission Pharmacal Company

San Antonio, Texas

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Pulse Biosciences

Hayward, California

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Plymouth Meeting, Pennsylvania

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Morristown, New Jersey

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Intrinsik

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San Diego, California

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Chesapeake Utilities Corporation

West Palm Beach or Fernandina Beach preferred, Florida

Theragent

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Duke Human Vaccine Institute

Durham, North Carolina

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Brisbane or Point Richmond, California

Duke Human Vaccine Institute

Durham, North Carolina

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Mirati Therapeutics

San Diego , California

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Regulatory Affairs Manager
Responsible for management of regulatory submissions and ongoing regulatory compliance for product development process.   Duties: Prepare and submit global regulatory applications, including U.S. Medical submissions (Pre· Submissions, 510ks, IDEs and applicable supplements and annual reports), Canadian Class 2 Device License submissions, EU MDR Submissions, and other International markets such as Japan, the Far East, Australia and Latin Review device labeling (Including IFU) and advertising materials for compliance with global regulations; analyze and recommends appropriate Review and signoff on design and manufacturing changes for compliance with applicable Support quality system audits by notified bodies, government agencies and


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