Connor Griggs
Regulatory Lead | Johnson & Johnson MedTech | Orthopaedics
Professional Overview
Connor Griggs is a seasoned Regulatory Lead with over 8 years of experience in the medical device and pharmaceutical industries. He specializes in navigating complex regulatory requirements, ensuring product compliance, and driving strategic initiatives to support business growth.
Experience Summary
Current Role
As the Regulatory Lead at Johnson & Johnson MedTech | Orthopaedics, Connor is responsible for overseeing the regulatory affairs function for a portfolio of orthopedic products. He directs the preparation and submission of regulatory filings, maintains strong relationships with global regulatory bodies, and collaborates cross-functionally to address emerging compliance needs. Under his leadership, the team has achieved a 95% first-time approval rate for new product submissions, significantly reducing time-to-market.
Career Progression
Prior to his current role, Connor held various regulatory positions, steadily advancing his expertise. As the Director of Business Development at Oriel STAT A MATRIX, he led a team of regulatory specialists in providing comprehensive consulting services to medical device and pharmaceutical clients, contributing to a 20% year-over-year revenue growth. As a Regulatory Project Manager at ARKRAY USA, he successfully managed the regulatory approval process for several in-vitro diagnostic devices, including the company's flagship glucose monitoring system. Earlier in his career, Connor gained valuable experience as a Regulatory Specialist at Boston Scientific and a Regulatory Coordinator at Smiths Medical, where he honed his skills in navigating global regulatory landscapes.
Academic Background
Connor holds a Bachelor of Science in Biomedical Engineering from the University of Minnesota, where he graduated cum laude. He is also a certified Regulatory Affairs Specialist (RAC) and actively participates in industry events and conferences to stay abreast of the latest regulatory trends and best practices.
Areas of Expertise
- Regulatory strategy and compliance
- Global regulatory submissions and approvals
- Quality systems and risk management
- Cross-functional collaboration and stakeholder management
- Project management and process optimization
Professional Impact
Throughout his career, Connor has made significant contributions to the medical device and pharmaceutical industries. He has led the successful regulatory approval of numerous innovative products, ensuring patient safety and timely market access. His expertise in navigating complex regulatory environments has enabled his employer organizations to maintain a competitive edge and expand their global footprint.
Conclusion
With his exceptional track record, Connor Griggs is a highly sought-after Regulatory Lead who consistently drives strategic initiatives and delivers measurable results. His ability to navigate the evolving regulatory landscape, coupled with his strong technical acumen and collaborative approach, make him a valuable asset to any organization in the medical device or pharmaceutical sector.
