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Opportunity to join a Class III Medical Device organization that manufacture complex life-saving cardiovascular devices. Having acquired competitors with equally-as-cool-tech, they're increasing their regulatory capacity with people motivated to advance their career and help battle coronary disease! Key Responsibilities Participating in defining regulatory strategies and submission activities (510(k), IDE, PMA, EU/CE Technical Documentation Files, Canadian…
Opportunity to join a local Connecticut Medical Devices manufacturer that are expanding their quality team due to an increase in their product portfolio! As part of the larger quality team, you'll have the chance to use your quality systems expertise to advise on new quality system process improvements and define procedures for the site! Responsibilities …