Principal Regulatory Affairs Specialist

Overview Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. The client seeks a Principal Regulatory Affairs Specialist to lead complex regulatory strategies and submissions for Class III implantable devices and software-driven technologies. Responsibilities Author and manage Original PMA submissions and PMA supplements. Drive regulatory strategy across the full product lifecycle (Premarket & Post-market). Ensure compliance for Class III medical devices, including software-embedded and SaMD products. Mentor and train junior regulatory professionals, fostering team growth and expertise. Collaborate cross-functionally to support global market access and regulatory excellence. Qualifications 7+ years of experience in Regulatory Affairs within the medical device industry. Proven experience authoring Original PMA and PMA supplements. Strong background in full-cycle Class III device regulatory processes. Experience with software-embedded or SaMD products. Demonstrated ability to mentor and develop junior team members. Ability to work on-site in a hybrid model (4 days per week). EOE EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. In addition to base pay, direct-hire employees may be eligible for client offered benefits such as medical, dental, and vision coverage, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change. To find out more about Real, please visit #J-18808-Ljbffr Real