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Senior Specialist, Regulatory Affairs

Stryker

Portage, MI · HybridJob$83–139K/yrPosted 1w agoSeen in employer's feed 6 days ago

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At a glance

Compensation
$83–139K/yr
Location
Portage, MIHybrid
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Stryker is seeking a Senior Specialist in Regulatory Affairs for its Smart Care team in Portage, Michigan. The role supports regulatory initiatives across product lifecycles, including software, sustaining, and environmental activities, partnering with cross‑functional teams to assess implications, guide compliance, and shape regulatory strategy to keep products globally compliant.

Skills & qualifications

RequiredNice to have

Skills

Regulatory AffairsRegulatory StrategyComplianceEnvironmental RegulationsSoftware as a Medical Device (SaMD)Risk-Benefit AssessmentProduct Lifecycle Management

Qualifications

Bachelor's Degree2 Years Experience in Regulatory AffairsExperience With Software Regulatory ActivitiesExperience With Environmental RegulationsExperience Supporting Full Product LifecycleRegulatory Affairs Certification (RAC)Master's Degree

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Stryker is hiring a Senior Specialist, Regulatory Affairs to join our Smart Care (https://www.stryker.com/us/en/smart-care.html) team. Join a team that supports regulatory initiatives across the product lifecycle, including software, sustaining, and environmental regulatory activities, to help ensure products remain compliant with applicable global regulatory requirements. This role partners with cross-functional teams to assess regulatory implications, support compliance and regulatory strategy activities, and provide regulatory guidance that informs product and business decisions.

Workplace Flexibility : Strong preference will be given to candidates who reside within a commutable distance of Portage, Michigan and can work a hybrid schedule.

What You Will Do

  • Support development, review, and maintenance of regulatory procedures and documentation.

  • Contribute to regulatory strategies and recommend updates based on evolving regulations, guidance, and industry standards.

  • Assess and support compliance with global regulatory and environmental requirements, evaluating potential impacts of evolving regulations on products, processes, and business activities.

  • Provide regulatory input for product development, lifecycle management, and change planning activities.

  • Evaluate regulatory requirements and potential impacts for new products, product modifications, and business initiatives.

  • Research and assess regulatory history, product classifications, and therapeutic or diagnostic landscapes to identify regulatory pathways and considerations.

  • Identify potential regulatory risks, trade-related considerations, and approval challenges, and communicate findings to project teams.

  • Define submission, registration, and approval requirements and support preparation of regulatory deliverables.

  • Participate in risk-benefit assessments and compare regulatory outcomes against original product concepts to support future recommendations and regulatory planning.

What You Will Need

Required Qualifications

  • Bachelor's degree required. Preferred in Regulatory Affairs, Engineering, Life Sciences, Biological Sciences, or a related field.

  • Minimum 2 years of experience in regulatory affairs within the medical device, biotechnology, pharmaceutical, healthcare industry, or other regulated industries.

Preferred Qualifications

  • Experience supporting regulatory activities for software products, including Software as a Medical Device (SaMD) and/or non-medical software solutions.

  • Experience assessing and supporting compliance with environmental regulations and reporting requirements.

  • Experience supporting products throughout the full product lifecycle, including development, commercialization, and post-market activities.

  • Regulatory Affairs Certification (RAC).

  • Master's degree in Regulatory Affairs, Engineering, Life Sciences, or a related discipline.

Posted Date: 09/01/2026

This role will be posted for a minimum of 3 days.

United States of America Pay Ranges:

  • USN : $83,300 - $138,800 USD Annual

  • US5 : $87,500 - $145,700 USD Annual

  • US10 : $91,600 - $152,700 USD Annual

  • US15 : $95,800 - $159,600 USD Annual

  • US20 : $100,000 - $166,600 USD Annual

  • US30 : $108,300 - $180,400 USD Annual

View the U.S. work location and transparency guide (https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) to find the pay range for your location.

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, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

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