Senior Regulatory Affairs Specialist

What you’d do

Manage regulatory submissions and reports for orthopedic medical devices, coordinate with product development, and review change requests. Full-time position in West Chester, PA. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• Bachelor's degree or equivalent
• 4-6 years work experience
• Excellent written and oral communication skills
• Ability to handle multiple tasks and be detail oriented