Job Opportunities API

What You’ll Do: • Train and mentor the Regulatory Affairs team on sources, resources, and the status of local, regional, and global regulations • Actively participate as a project stakeholder, driving value and meeting planned milestones • Develop, update, and lead global regulatory strategies and Regulatory Plans for projects • Prepare, submit, and track regulatory applications under review; provide updates to project teams independently • Negotiate with regulatory authorities on common issues throughout the submission process • Perform and oversee regulatory impact assessments of post-market changes • Act as an independent reviewer for peer submissions • Support global registration activities by providing data, developing documentation, and coordinating information requests • Monitor the regulatory environment and share relevant updates with the broader RA team • Review and approve collateral materials, Medical Education materials, and presentations • Actively participate in and support external audits • Execute acquisition integration strategy post-close under limited supervision • Drive process improvements and recommend changes to procedures • Advise on regulatory requirements for quality, preclinical, and clinical data in support of submissions and clinical study applications • Evaluate proposed preclinical, clinical, and manufacturing changes for regulatory filing strategies • Ensure compliance with post-approval/clearance requirements, labeling, advertising, and promotional materials What You Bring: • Bachelor’s degree (B.A. or B.S.) in Science, Legal, Regulatory, Engineering, or equivalent • RAC certification preferred • Minimum of 7 years of regulatory experience in the medical device or pharmaceutical industry • Demonstrated knowledge and skills in regulatory pathways, risk-benefit analysis, submissions, registration, compliance, post-market surveillance, and distribution • Ability to operate with appreciable latitude for independent action and decision-making • Experience planning, conducting, and overseeing regulatory assignments with limited supervision • Strong communication, collaboration, and stakeholder management skills • Ability to mentor and potentially oversee the work of Specialists or Senior Specialists • Willingness to accept challenging assignments that stretch and build capabilities Why VB Spine? We believe in growing talent from within. At VB Spine, join a high-performing Regulatory Affairs team where you’ll provide senior-level strategic guidance that enables the successful global launch and continued compliance of innovative spinal technologies. Compensation: Pay for this role is competitive and based on experience, qualifications, and performance. The typical pay range for this position is $135,000.00 - $145,000.00 annually, with potential for bonuses and incentives plus benefits. Final compensation is determined on a case-by-case basis and considers a variety of factors including experience level, regulatory expertise, and market conditions. Benefits include: • Comprehensive health, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) and holidays • Ongoing training and professional development opportunities • Opportunity to grow within a fast-paced, dynamic company Sr. Staff Regulatory Affairs Specialist Location: Allendale, NJ, Leesburg, VA, or Remote Company: VB Spine Looking for a career where your work truly matters? At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We’re the largest privately held spine company and among the largest family-owned medical technology companies in the world, dedicated to innovation, surgeon partnerships, and improving patient outcomes in spine care. As a Principal Regulatory Affairs Specialist in our Regulatory Affairs function within the Spine division, you’ll apply broad and advanced knowledge of regulatory frameworks, requirements, and processes to advise cross-functional teams and leadership on complex projects and strategies — supporting global product development, lifecycle management, and regulatory