Hybrid Principal Regulatory Affairs Lead, Medical Devices

West Pharmaceutical Services in Exton, PA seeks a Principal Specialist, Regulatory Affairs (Medical Devices) to influence regulatory strategies and oversee global submissions, including US FDA 510(k) and EU MDR documentation for new products and changes. The role partners with QA, R&D and manufacturing to ensure compliant, timely submissions, mentors team members, and supports regulatory requests from internal and external customers while maintaining compliance with applicable regulations.
This is a strong opening to take on the Hybrid Principal Regulatory Affairs Lead, Medical Devices role at West Pharmaceutical Services. Full responsibilities and requirements are described in the listing above. Learn more about the Hybrid Principal Regulatory Affairs Lead, Medical Devices role in the description above. We appreciate your interest in this position. Join West Pharmaceutical Services and contribute to our ongoing work.