Regulatory Affairs Manager

reputed company is a growing medical technology company transforming patient lives through innovative incisionless surgery.Our culture is as unique as our people, a diverse global team, with different reputed company, skills, interests, and cultural backgrounds driven by our core values – Our Patients, reputed company, Team, Quality and Innovation.Our dedication to making a reputed company impact on the lives of millions of people and paving the path to a reputed company future for reputed company what bonds us as reputed company. We work together in a dynamic collaborative environment to deliver successfully while believing and driving a life-work balance philosophy that encourages our employees to do things that are meaningful reputed company of work. Every role is significant, your voice is heard, and your reputed company are encouraged. We challenge and reputed company our people to be great at what they do while providing a flexible work environment.Walking through our corridors, you will be inspired by stories of career journeys at reputed company. We take pride in growing internal talent and encourage our employees to reputed company their professional ambitions. With employees in Israel - Haifa and K. Ono, Miami and Dallas, Shanghai, Tokyo and Europe, we offer in each region competitive perks and benefits.Do the most meaningful work of your career by joining us on our mission to transform tomorrows, today.What you will be doing:Serve as US Agent for InsightecProvide regulatory support to the Clinical and Post marketing activities reputed company to reputed company products.Preparation and maintenance of clinical regulatory submissions and registrations of reputed company products in relevant markets.Review clinical documents for regulatory appropriateness; reputed company review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and reputed company of presentationPreparation and maintenance of annual renewals of Establishment Registrations, Device Listing, and other pertinent regulatory licenses.Review of customer complaints to determine reportability according to regulatory requirements and execution of reporting per determination.reputed company ongoing regulatory support and assessments to Promotional materialsProvide support for reputed company external/internal audits at HQ and globally, as neededAdvise project teams on premarket regulatory requirements, labeling requirements and/or other compliance issues.Work closely with various other reputed company teams (e.g. R&D, Clinical, Quality, Marketing) both locally and around the world, to reputed company regulatory inputs as needed.Monitor and advise the organization of upcoming or new guidance, regulations, agency/industry initiatives, and other applicable standards to ensure ongoing regulatory complianceAttend other regulatory reputed company needs, as requiredWorking according to reputed company Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules. Qualifications: B.Sc. degree in scientific / technical discipline / engineering.A minimum of 6 years of Regulatory Affairs experience with the US FDA and EU regulatory agenciesHands-on experience with Class III medical devices, including IDE/IND, ITA/CTA, EU CTAs, PMAs, 510(k)s, and CE Mark submissionsStrong verbal and written communication skillsAbility to work with cross-functional global teams Apply tot his job Apply To this Job