Bachelor's degree in a scientific or technical discipline preferred.
2+ years in Regulatory Affairs or 3 years in related fields like R&D, Quality, or Clinical.
Introductory knowledge of FDA and EU regulations required.
Proficient in Microsoft Office Suite including Word, Excel, and PowerPoint.
Responsibilities
Support Regulatory Affairs for compliance during product development and engineering projects.
Coordinate and submit regulatory filings for product variations, including PMAs and 510(k)s.
Develop regulatory strategies for new and modified products.
Act as a core team member providing regulatory guidance during product development and commercialization.
Communicate with device reviewers to establish relationships and clarify submission strategies.
Review design changes for compliance with regulations.
Facilitate interactions with regulatory agencies during submission reviews and audits.
Benefits
Comprehensive health insurance plans.
Retirement savings options with company matching.
Generous paid time off and holiday schedule.
Opportunities for professional development and continuing education.
Full Job Description
Responsibilities:
This role is responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process and sustaining engineering projects, ensuring compliance with FDA and EU regulations, ISO standards, and other regulatory agencies
Coordinate, compile, and submit US and EU regulatory filings for new and modified products, including PMAs, PMA supplements, pre-submissions, 510(k)s, annual reports, and MDR CE mark submissions
Develop and implement regulatory strategies for new and modified products
ct as a core team member on sustaining and new product development projects, providing regulatory feedback and guidance throughout the product and manufacturing process development cycle, commercialization, and coordinating team inputs for submissions
ct as a company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow-up of submissions under review
Review and approve design and manufacturing changes for existing products, ensuring compliance with applicable regulations
Interact with regulatory agencies as part of submission review and on-site audit support
Review device labeling for compliance with global regulations; analyze and recommend appropriate changes
Support and maintain Quality initiatives in accordance with BSC Quality Policy
Participate in development and implementation of departmental policies and procedures
Foster a work environment of continuous improvement that supports BSC's Quality Policy, Quality System and the appropriate regulations for their area of responsibility
Requirements:
minimum of a bachelor's degree, preferably in a scientific or technical discipline.
minimum of 2-year work experience in Regulatory Affairs or 3 years' work experience in a related discipline (e.g., R&D, Quality, Clinical, Medical Affairs, Biocompatibility) in the medical device industry.
Introductory knowledge of FDA, EU and/or international regulations.
Proficiency with Microsoft Office applications (Word, Excel, PowerPoint, Teams, SharePoint, MS Forms).
