Senior Regulatory Affairs Specialist
Boston Scientific
Senior Regulatory Affairs SpecialistWork mode: Hybrid Onsite Location(s): Marlborough, MA, US, 01752 Additional Location(s): US-CA-Irvine; US-MN-Arden Hills; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing – whatever your ambitions.About this role: At 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.Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. 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. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.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 supervisionThe anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. Boston Scientific
$92k - $138k
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$99.7k - $152.08k
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...Senior International Regulatory Affairs Specialist Irvine, CA Join a team focused on bringing medical technologies to market while ensuring compliance with global regulatory requirements. In this role, you will support regulatory strategy, submissions, and product...SeniorFull timeLocal area$32.5 - $36 per hour
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$60 per hour
Our client, a leading organization in the medical device and diagnostics industry, is seeking a Regulatory Affairs Specialist to join their team. As a Regulatory Affairs Specialist, you will be part of the Regulatory Affairs department supporting global product registration...Hourly payTemporary workMonday to FridayShift work- ..., medical technology or similar.5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the... ...communication skills.Thorough knowledge of policies, practices and procedures related to Regulatory Affairs. Katalyst HealthCares & Life Sciences
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Baker Tilly US is seeking an experienced professional for transaction advisory services in Irvine, California. The role involves managing due diligence, client communication, and financial analysis, making it essential to have at least 8 years of relevant experience and...Senior- ...individuals, partnerships, corporations, and trusts; also reviews related income tax workpapers. Supervises teams of staff accountants. Plans, organizes and implements income tax returns. Coaches Tax Accountant, Tax, Staff Accountant, Accountant, Senior, Staffing, Accounting...Senior
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