Jobs · Legal

Staff Regulatory Affairs Specialist (Remote)

Stryker · United States · 1 wk ago
RemoteRemoteLegal$78k–$130k/yrFull-time

About the role

This remote position supports Stryker’s Neurovascular division, focusing on bringing new medical devices to market while ensuring ongoing compliance. You will participate on cross-functional teams, develop global regulatory strategies, author regulatory submissions, and interact with regulatory agencies/notified bodies in major markets including the US, EU, Canada, Japan, China, Australia, Brazil, and more.

Responsibilities

  • Develop and execute regulatory strategies for pre-market products to achieve market access across global regions.
  • Evaluate regulatory requirements and identify submission pathways for new products, ensuring alignment with applicable regulations.
  • Author and submit regulatory documents, including FDA submissions and international dossiers, to support product approvals.
  • Assess global regulatory impact of product or process changes and coordinate required notifications or submissions.
  • Partner with cross-functional teams to support regulatory agency interactions, including responses, meetings, and documentation.
  • Monitor regulatory intelligence and implement updates to strategies based on evolving global requirements.
  • Maintain and update standard operating procedures to ensure compliance and improve regulatory processes.
  • Provide regulatory guidance to stakeholders to align product lifecycle activities with applicable standards.

Requirements

  • Bachelor’s Degree (B.S. or B.A.)
  • Minimum 4 years of experience in an FDA-regulated industry
  • Minimum 2 years of experience in regulatory affairs
  • Demonstrated applied knowledge of FDA and international medical device regulations/standards (e.g., EU MDR)

Preferred Qualifications

  • Bachelor’s degree in engineering, science, or related field
  • Regulatory Affairs Certification (RAC) or advanced degree in regulatory affairs or related discipline
  • Experience with Class II or Class III medical devices
  • Experience authoring 510(k) submissions or equivalent regulatory filings
  • Experience interacting with regulatory agencies or supporting regulatory meetings

Pay

  • Puerto Rico: $77,700 - $129,500 USD Annual
  • USN: $95,700 - $159,500 USD Annual
  • US5: $100,500 - $167,500 USD Annual
  • US10: $105,300 - $175,500 USD Annual
  • US15: $110,100 - $183,400 USD Annual
  • US20: $114,800 - $191,400 USD Annual
  • US30: $124,400 - $207,400 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.

Benefits

Health benefits include:

  • Medical and prescription drug insurance
  • Dental insurance
  • Vision insurance
  • Critical illness insurance
  • Accident insurance
  • Hospital indemnity insurance
  • Personalized healthcare support
  • Wellbeing program and tobacco cessation program

Financial benefits include:

  • Health Savings Account (HSA)
  • Flexible Spending Accounts (FSAs)
  • 401(k) plan
  • Employee Stock Purchase Plan (ESPP)
  • Basic life and AD&D insurance
  • Short-term disability insurance

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