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Job description
West Pharmaceutical Services, Inc. seeks a Principal/Manager, Regulatory Affairs (Medical Devices) to lead regulatory strategies for worldwide submissions, including US FDA and international requirements. The role mentors staff and collaborates across RA, QA, and R&D to ensure compliant submissions and timely approvals for new products and changes.
Hybrid work model; onsite minimum 3 days/week. Requires 8+ years in medical device regulatory affairs, RAC preferred, and strong written/spoken
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Worksite address
scottsdale, AZ, 85261, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.