Principal Regulatory Affairs Specialist
Principal Regulatory Affairs Specialist
Posted on :
11-07-2025
Employer Active
1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
11-07-2025
Job Description
Company Overview
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 PROCEPTs 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
The Qualifications We Need You to Possess
- Bachelors degree in a scientific discipline; advanced degree and RAC (Regulatory Affairs Certificate) preferred
- Minimum of 10 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
$172000 - $234000 a year
Understanding PROCEPTs Culture
At PROCEPT we believe every person matters. Every employee every patient every caregiver. Because we are here to create a revolution and we believe in doing that by innovating everywhere with pathological optimism. We believe in being humble and highly engaged in the work we do while also working together seamlessly for a common goal. At Procept curiosity ingenuity and conviction in the power technology will transform the lives of our patients and providers.
And this doesnt happen by accident. It starts with our live induction program that serves as an incubator for cross-functional team building an immersion in Procepts history jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do. It continues with our one-of-a-kind management program designed to build the best managers in the industry where our people managers across functions come together to exchange ideas and grow as both managers and learners in an environment that challenges supports and broadens.
We are fueled by the opportunity to give people their lives back. And we believe that it begins with YOU! At Procept we push beyond just finding a work/life balance we strive to find a work/life blend a professional world that you are honored and impassioned to belong to one that you can proudly share with your family friends and acquaintances.
An opportunity at PROCEPT BioRobotics wont just be about finding a job. It will be an opportunity for you to join a community devoted to making a difference in this world!
BENEFITS OF WORKING AT PROCEPT!
PROCEPTs health and wellness benefits for employees are second to none in the industry. As an organization one of our top priorities is to maintain the health and wellbeing of our employees and their families. We offer a comprehensive benefits package that includes full medical coverage wellness programs on-site gym a 401(k) plan with employer match short-term and long-term disability coverage basic life insurance wellbeing benefits flexible or paid time off paid parental leave paid holidays and many more!
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT
PROCEPT BioRobotics is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind on the basis of race color national origin religion gender gender identity sexual orientation disability genetic information pregnancy age or any other protected status set forth in federal state or local laws. This policy applies to all employment practices within our organization.
PAY RANGE TRANSPARENCY
Procept is committed to fair and equitable compensation practices. The pay range(s) for this role represents a base salary range for non-commissionable roles or on-target earnings for commissionable roles. Actual compensation packages are based on several factors that are unique to each candidate including but not limited to job-related skills depth of experience relevant certifications and training and specific work location. Based on the factors above Procept utilizes the full width of the range. The total compensation package for this position may also include eligibility for annual performance bonus equity and the benefits listed above.
WORK ENVIRONMENT
Well provide you training for and ask you to maintain trained status for and comply with all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance. We would also ask you to understand and adhere to the PROCEPT BioRobotics Quality & EHS policies.
Required Experience:
Staff IC
Employment Type
Full-Time
Key Skills
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