Principal Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. We are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.

The Opportunity That Awaits You:

The Principal Regulatory Affairs Specialist provides regulatory leadership for product manufactured by PROCEPT BioRobotics ("company") from development through marketing approval and commercialization. Responsibilities include coordination and preparation of regulatory submissions and for the development/revision of procedures and practices to ensure compliance with FDA and international regulations, guidelines, and standards, and providing regulatory guidance to project teams.

The initial role of the Principal Regulatory Affairs Specialist will be as an individual contributor, reports to the Senior Director of Global Regulatory Affairs.

The ideal candidate would have had previous medical device experience and looking for potential for growth.

What Your Day-To-Day Will Involve:

• Regulatory representation and leadership to cross-functional products teams, development of regulatory strategies and support PROCEPT's products, marketing applications and post-market activities
• Providing training, coaching and mentoring to other regulatory affairs specialists
• Assisting in strategic decision making, and representing regulatory at all levels of the business
• Responsible for project timelines and management of regulatory submissions including preparing IDE, 510K and international submissions for new products, new indications, and significant product changes, to ensure compliance with the FDA and international regulations and guidelines
• Prepare Letters to File documentation to support internal filings for product development projects and product changes not requiring regulatory agency approvals
• Prepare and maintain Technical Files/Technical Documentation for Europe (CE Mark) for new products, new indications, and significant product changes
• Support product development teams on regulatory issues, including review of documentation
• Provide regulatory assessments for anticipated design, manufacturing, and labeling changes
• Represent RA functional area in the review and approval of Engineering Change Orders (ECO)
• Provide regulatory guidance with regard to the preparation, review and approval of labeling and promotional materials
• Perform regulatory research and stay abreast of changes for US and international regulations and requirements
• Provide regulatory support for quality assurance and regulatory compliance activities as required
• Maintain well-organized, auditable regulatory files
• Maintain trained status for, and comply with, all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance
• Understand and adhere to the PROCEPT BioRobotics EHS Policy

The Qualifications We Need You to Possess

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Qualifications / Skills Required

• Bachelor's degree in a scientific discipline; advanced degree and RAC (Regulatory Affairs Certificate) preferred
• Minimum of 12 years' experience in medical device industry with experience in regulatory affairs with direct submissions responsibilities
• Knowledge of relevant Title 21 of the US code of Federal Regulations is required
• Experience with US Federal Food, Drug, and Cosmetic Act (FD&C) Section 510(k) is required
• Experience with European Medical Device Directive (93/42/EEC with 2007/47/EC) is required
• Experience with Quality Management System Standard ISO 13485 is required
• Experience with Risk Management Standard ISO 14971 is required
• Knowledge of EU MDR regulations is required
• Knowledge of International Medical Device requirements (Canada, Australia, New Zealand, China, Japan, etc.) is preferred
• Proficiency in basic computer skills, including Microsoft Office Suite (Word, PowerPoint and Excel) and Adobe Acrobat
• Strong organization skills, able to manage multiple projects and timelines
• Competence in applying scientific principles and logical thought processes in preparing regulatory documentation
• Excellent oral and written communication skills
• Strong attention to detail
• Ability to work independently as an individual contributor and in a team environment
• Knowledge of software development and software quality as it relates to regulatory submissions a plus