SENIOR REGULATORY AFFAIRS SPECIALIST

Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist.  Remote work options may be considered on a case-by-case basis and if approved by the Company Abiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives.
Abiomed's "Patients First!" culture drives our skilled workforce and strong relationships with clinicians.
Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.
Founded in , Abiomed has a proven track record for growth, integrity and innovation.
The Senior Regulatory Affairs Specialist will be responsible for developing strategies to obtain FDA clearance or approval of new Class II & III cardiovascular medical devices and improvements to existing devices.
You will advise on regulatory requirements as a key member of cross-functional teams, prepare and review FDA submissions, and interact with and respond to FDA pre-submission and during the review period.
Through your engagement in this role, you will help shape the life-saving field of heart recovery.  The ideal candidate will.
·       Be passionate about Regulatory Affairs impact in support of the research, development, clinical, marketing, and production of state-of-the-art class III cardiovascular medical devices ·       Be energized by joining a world-class company and regulatory team ·       Enjoy teamwork and thrive as a member of dynamic cross-functional teams ·       Build and maintain strong interpersonal relationships within and outside of the company ·       Exhibit leadership traits- positive, forward looking, accountable, action-oriented, delivering results ·       Adaptable and thrive in a dynamic work environment where variety is the routine.
·       Embrace change, continuous learning, and work skills improvement Key Responsibilities.
·       Support cross-functional new product development projects and lead compilation of all materials required for submissions to FDA ·       Provide ongoing support to project teams for regulatory issues and questions.
Find, interpret and apply regulations and guidance appropriately for situations ·       Provide regulatory support for currently marketed products as necessary to ensure ongoing compliance ·       Provide support for changes to existing products, including providing regulatory assessment of changes, and subsequent regulatory filings ·       Develop solutions to a variety of technical problems.
Actively participate in problem solving discussions and recommend solutions ·       Keep abreast of FDA guidance documents and regulations and monitor impact of changing regulations on submission strategies ·       Assist in the maintenance and improvement of regulatory SOPs ·       Interact and negotiate with regulatory agencies on defined matters as needed Qualifications Education ·       Degree in engineering or science required ·       Advanced degree is preferred Required ·       Minimum of 4 years with a Bachelor's degree  or Minimum of 3 years with an advanced degree ·       Regulatory affairs experience in the medical device industry with a track record of successful submissions ·       Experience in reviews of engineering, manufacturing, marketing, labeling and clinical documents for regulatory compliance ·       History of successful IDE/PMA/510(k) device submissions (Class III device submissions preferred) ·       Experience supporting software device development (for example SiMD, SaMD, AI, Cybersecurity, IEC etc) ·       Experience with FDA requirements, guidance documents, ISO , ISO , IEC , IEC ·       Ability to effectively manage multiple projects and priorities ·       Strong communication and regulatory writing skills ·       Strong problem solving skills, interpersonal skills and effective team member ·       Results oriented.
Ability to drive to completion in adherence to aggressive project schedules Preferred ·       Ability to comprehend principles of engineering, physiology and medical device use.
Cardiovascular device experience ·       Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society) Other ·       Travel up to 10% ·       Must be able to effectively work remotely This job posting is anticipated to close on .
The Company may however extend this time-period, in which case the posting will remain available on https://www.
areers.
nj.
om to accept additional applications.  For U.
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applicants, in accordance with applicable disclosure requirements, the anticipated base pay range for this position is $ to $.
The Company maintains highly competitive, performance-based compensation programs. .  Additional information can be found through the link below. For additional general information on company benefits, please go to.
https://www.
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om/employee-benefits Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.