Senior Regulatory Affairs Specialist

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.We foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.Position SummaryThe Senior Regulatory Affairs Specialist originates appropriate documents to obtain and maintain marketing privileges consistent with applicable government requirements where AtriCure conducts business. This position will prepare and submit submissions, which may include US device 510(k), PMA Supplements, EU, Canada, Australia, Brazilian, Japanese, and other international submissions to support business growth. The position will serve as regulatory representative on selected projects for new product development or line extension and will provide regulatory supervision on post-market product changes to maintain marketing approvals.Essential Functions Of The PositionPrepare written regulatory strategies for new product development and sustaining projectsPrepare US submissions as necessary including 510(k) regulatory applications, PMA supplements for device and manufacturing, drafting 510(k) letters to file to secure/maintain marketing approvalsPrepare EU, Canada, Australia, Brazilian, Japanese, and other international submissions or notifications of change when necessaryRepresent Regulatory Affairs as core team member of new product development projects to drive innovation and to support Design Control processProvide Regulatory support for risk management activities and clinical evaluationDevelop Regulatory Strategies for new or modified products and assist on project planningAct as the Regulatory liaison with key agency stakeholders including FDA, EU Notified Body, Health Canada, and other government agencies on behalf of the organization to facilitate timely and favorable review of submissions and pre-submission activityCollaborate with regional regulatory personnel on assessing and documenting the global impact of product change on product registration and license globallyAssist in development/maintenance of regulatory operational practicesSupports inspections and audits by FDA, notified body, and other regulatory agenciesMonitor and provide management with impact of changes in the Regulatory environmentConducts reviews and provides input to the development of technical documentation including test reports across multiple disciplines including sterilization, biocompatibility, and electrical safety.Plans coordinate and compile submissions with minimal review and with sign-off responsibilityDemonstrate strong working knowledge of global laws, regulations, guidelines, and standards related to commercialization and post market surveillanceMaintain current knowledge base on existing and emerging regulations, standards, and guidance documents and apply them to change control sign-offsIndependently manage multiple projects, department initiatives, and day-to-day tasksDemonstrate strong working knowledge of clinical technical concepts and applications related to commercialized productsAdditional Essential Functions Of The PositionRegular and predictable work performanceAbility to work under fast-paced conditionsAbility to make decisions and use good judgementAbility to prioritize various duties and multitask as requiredAbility to successfully work with othersAdditional duties as assignedAbility to coordinate projects, track milestones and communicate progress to stakeholderBasic QualificationsBachelor’s degree required or demonstrated equivalent combination of education, training and experienceA minimum of 4 years of regulatory affairs working experience, mainly for medical devices.Must have knowledge of U.S. and/or European/International regulations and standardsExperience in preparing regulatory submissions; Experience interacting with FDA and/or other regulatory agenciesProvide examples of past approvals/clearances with regulatory agencies.Must demonstrate good technical writing skill; Must work well in team environments; Must demonstrate good communication skill in team settingProficient on programs within Microsoft Office; Proven analytical abilities, Solid understanding of manufacturing and change control, and an awareness of regulatory trendsAbility to travel 10-15%Preferred Qualifications4-year degree in a technical/scientific disciplineWorking experience with cardiac devices, including capital equipmentExperience with medical capital equipment with embedded software and knowledge of electrical device standards, ie. Electrical Safety (IEC 60601-1) and EMCOther RequirementsAbility to regularly walk, sit, or stand as neededAbility to occasionally bend and push/pull as neededAbility to pass pre-employment drug screen and background checkPositions in MinnesotaMinnesota pay range$106,000—$130,000 USDAtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.AtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https://www.e-verify.gov AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).You may access our global privacy policy here: https://www.atricure.com/privacy#LI-JH1