Senior Regulatory Affairs Specialist

Senior Regulatory Affairs SpecialistAt Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work. We offer a collaborative culture that values diversity and prioritizes initiatives that promote awareness and inclusion, celebrating personal, cultural, and demographic differences of our customers, patients, and workforce. In the Urology division, we continually advance the quality of patient care with innovative Urology solutions.We are looking to hire an enthusiastic individual for a Senior Regulatory Affairs Specialist position (hybrid work mode) supporting our rapidly growing active implantable device portfolio. This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies. The role requires strong US, EU, and international regulatory experience that can be leveraged to help support international expansion. In this role, you'll be part of a high-functioning, close-knit Regulatory Affairs team responsible for support of submissions and on-going regulatory compliance through partnership with our global R&D, manufacturing, clinical, and quality teams.This role follows a hybrid work model requiring employees to be in our local office at least three days per week. We will consider candidates from the following office locations: Irvine, CA, Marlborough, MA, Arden Hills, MN, or Maple Grove, MN.Your responsibilities will include:Reviews change notifications and performs regulatory impact assessment for product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings, and supports associated global submissions as neededSupports the coordination, drafting, and submitting of U.S. and EU regulatory filings for new and modified Class III productsProvides technical reviews of test protocols and reportsAssesses labeling materials, including Instructions for UseRepresents RA on cross functional project teamsWorks as liaison with International BSC Regulatory colleagues on various projects, including providing support with international regulatory filingsSupports highly technical or major business segment product lines, special projects or strategic initiativesRequired Qualifications:A minimum of a Bachelor's Degree in a scientific, technical, or related disciplineA minimum of 4 years Regulatory Affairs experience in the medical industryPrior experience with 510(k) submissions, EU MDR or international regulatory registrationsPreferred Qualifications:Prior experience with PMA submissions or Class III submissionsPrior experience with active implantable devices, active devices, or long-term implants.Working knowledge of FDA, EU and international regulations for medical devicesGeneral understanding of product development process, design control and quality system regulationsAbility to simultaneously manage several projectsProficiency with Microsoft OfficeEffective research and analytical skillsEffective written and oral communication, technical writing and editing skillsAbility to work independently with minimal supervisionCompensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs.