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Senior Regulatory Affairs Specialist image - Rise Careers
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Senior Regulatory Affairs Specialist - job 1 of 2

Job Summary

A company is looking for a Senior Regulatory Affairs Specialist, Program Lead.

Key Responsibilities
  • Author regulatory submissions and support product development for US and international regulatory approval
  • Manage and prepare regulatory submissions for device approvals and registrations globally
  • Function as a Regulatory Affairs subject matter expert supporting cross-functional partners through design control activities
Required Qualifications
  • Master's degree in Pharmacy Administration, Biomechanical Engineering, or a related field
  • 4 years of experience in regulatory affairs or a related occupation
  • Experience with regulatory submissions and health authority communications
  • Knowledge of regulatory requirements for medical devices
  • Experience in cross-functional collaboration in product development

Average salary estimate

$100000 / YEARLY (est.)
min
max
$80000K
$120000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

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MATCH
VIEW MATCH
FUNDING
DEPARTMENTS
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
No info
EMPLOYMENT TYPE
Full-time, remote
DATE POSTED
May 31, 2025

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