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Stryker Medical Devices Jobs (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Senior Staff Medical Writer (Remote)

San Diego, CA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Senior Staff Medical Writer (Remote)

Denver, CO · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Senior Staff Medical Writer (Remote)

Phoenix, AZ · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Senior Staff Medical Writer (Remote)

Los Angeles, CA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Senior Staff Medical Writer (Remote)

Seattle, WA · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals ...

Stryker

Staff Engineer - Sage, NPD

Cary, IL · Hybrid

$98K - $163K/yr

Sage | Stryker. What You Will Do * Design, develop, and verify components and subsystems for medical devices with minimal supervision. * Translate user needs into design specifications and deliver ...

Stryker

Staff Engineer - Sage, NPD

Cary, IL · On-site

$98K - $163K/yr

Sage | Stryker. What You Will Do * Design, develop, and verify components and subsystems for medical devices with minimal supervision. * Translate user needs into design specifications and deliver ...

Stryker

Senior Engineer - Sage, NPD

Cary, IL · Hybrid

$85K - $142K/yr

Sage | Stryker. What You Will Do * Research, design, develop, modify, and verify mechanical components and modules for medical devices with minimal supervision. * Translate design inputs into ...

Stryker

Repair Specialist

San Jose, CA · On-site

$26.11 - $32.87/hr

As a Repair Specialist on Stryker's ProCare team, you will perform high-quality repairs of medical devices while supporting daily production goals in a team-based environment. You will work ...

Stryker

Repair Specialist

San Jose, CA · On-site

$26.11 - $32.87/hr

As a Repair Specialist on Stryker's ProCare team, you will perform high-quality repairs of medical devices while supporting daily production goals in a team-based environment. You will work ...

Stryker

Senior Engineer - Sage, NPD

Cary, IL · On-site

$85K - $142K/yr

Sage | Stryker. What You Will Do * Research, design, develop, modify, and verify mechanical components and modules for medical devices with minimal supervision. * Translate design inputs into ...

Stryker Group

Staff Engineer - Sage, NPD

Cary, IL · On-site

$98 - $164/hr

Sage | Stryker. What You Will Do * Design, develop, and verify components and subsystems for medical devices with minimal supervision. * Translate user needs into design specifications and deliver ...

Stryker

Staff Software Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

Hybrid Join a team developing embedded software for advanced electromechanical medical devices within Stryker's Orthopaedic Instruments business. In this role, you will contribute to software systems ...

Stryker Group

Senior Engineer - Sage, NPD

Cary, IL · On-site

$86 - $143/hr

Sage | Stryker. What You Will Do * Research, design, develop, modify, and verify mechanical components and modules for medical devices with minimal supervision. * Translate design inputs into ...

Stryker

Staff Software Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

Hybrid Join a team developing embedded software for advanced electromechanical medical devices within Stryker's Orthopaedic Instruments business. In this role, you will contribute to software systems ...

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Stryker Medical Devices information

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$24K

$58.4K

$135K

How much do stryker medical devices jobs pay per year?

As of Aug 25, 2026, the average yearly pay for stryker medical devices in the United States is $58,439.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,500.00 and $69,500.00 per year, depending on experience, location, and employer.

What is a Stryker Medical Devices job?

A Stryker Medical Devices job typically involves working for Stryker Corporation, a leading medical technology company that designs and manufactures medical devices, equipment, and implants. Employees in these roles may work in sales, engineering, manufacturing, regulatory affairs, or customer support. Responsibilities depend on the specific job but often include developing, selling, or supporting innovative medical products used in hospitals, surgical centers, and other healthcare settings. Stryker is known for its strong company culture, career growth opportunities, and focus on improving patient outcomes.

What are the typical daily responsibilities for a Stryker Medical Devices professional?

Professionals at Stryker Medical Devices often spend their days engaging with healthcare providers, delivering product demonstrations, providing technical support, and training clinical staff on device usage. Responsibilities may also include attending surgeries or procedures to offer guidance, troubleshooting device issues, and maintaining compliance with industry regulations. Collaboration with sales, engineering, and customer service teams is common, ensuring a smooth customer experience and timely resolution of client needs. This dynamic environment offers continual learning opportunities and direct impact on patient care outcomes.

What are the key skills and qualifications needed to thrive in a Stryker Medical Devices position?

To excel in a role at Stryker Medical Devices, you should have a background in biomedical engineering, sales, or healthcare along with in-depth knowledge of medical devices and industry regulations. Familiarity with CRM software, device tracking systems, and certifications such as Certified Sales Professional (CSP) or relevant clinical credentials are greatly valued. Excellent communication, relationship-building, and problem-solving skills are essential for effectively supporting healthcare clients and collaborating with cross-functional teams. These skills and qualifications ensure safe device operation, regulatory compliance, and exceptional customer support in a dynamic, innovation-driven environment.

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Stryker Medical Devices jobs near you
Infographic showing various Stryker Medical Devices job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $58,439 per year, or $28.1 per hour.

Senior Compliance Engineer - Digital Health, Connected Medical Devices

Portage Des Sioux, MO • On-site

Jobtailor
See more jobs at Jobtailorexternal

$95 - $140/hr

Other

Posted 7 days ago

Job description

Responsibilities
  • Provide dedicated compliance engineering support for Stryker Medical’s Smart Care portfolio of software as/in a Medical Device, hardware, sensors, and customer applications
  • Lead product compliance strategy for new product development and sustaining engineering activities
  • Translate global regulatory and compliance requirements into design inputs, verification plans, and market access strategies
  • Drive compliance activities from concept development through verification, validation, and commercialization
  • Assess compliance risks, predicate product considerations, and emerging requirements
  • Integrate compliance requirements into system architecture, product design, and technology roadmaps
  • Define compliance test strategies, methods, operating environments, and worst-case conditions
  • Manage external testing laboratories, certification bodies, and third-party partners for global certifications and regulatory submissions
  • Serve as a technical compliance subject matter expert during design reviews, risk assessments, and development activities
  • Support procedure development, technical reviews, innovation opportunities, and cross-business initiatives
  • Collaborate with stakeholders and business units to align compliance strategies with user needs, product classifications, and market requirements
Requirements
  • Bachelor’s degree in Computer Science, Software Engineering, Electrical Engineering, or related discipline
  • 4+ years of compliance engineering experience required
  • Experience with product safety regulatory certification for major standards bodies and frameworks, including IEC 60601-1, IEC 60601-1-8, FCC Requirements, and IEC 62368-1
  • Experience with medical device product development lifecycle, including design controls and risk management
  • Experience working with and managing third-party certification laboratories such as UL, TÜV, CSA, and Intertek
  • Experience with device regulatory certification involving safety, EMC, and/or wireless standards
  • Knowledge of telecom/non-medical device standards
  • Familiarity with different software development life cycles
  • Basic knowledge of regulatory certification and device submission processes
  • Ability to work independently and effectively in a matrixed organization
  • Ability to work cross-functionally with Research & Development, Regulatory Affairs, and Marketing
  • Strong written, verbal, and interpersonal communication skills with the ability to influence without authority
Core Competencies

Demonstrates expertise in compliance engineering for medical devices, including regulatory certification processes and product safety standards. Proficient in managing compliance activities throughout the product development lifecycle while collaborating cross-functionally to align strategies with market requirements.

Highest-signal resume keywords
  • Compliance Engineering Experience
  • Regulatory Certification Knowledge
  • Product Safety Standards Expertise
  • Medical Device Development Lifecycle
  • Cross-Functional Collaboration
ATS Optimization Keywords Hard Skills
  • Compliance Engineering
  • Regulatory Certification
  • Risk Management
  • Design Controls
  • IEC 60601-1
  • IEC 60601-1-8
  • FCC Requirements
  • IEC 62368-1
  • Device Submission Processes
  • Telecom Standards
Soft Skills
  • Strong Communication Skills
  • Influencing Without Authority
  • Independent Work
  • Cross-Functional Teamwork
Industry Keywords
  • Medical Device
  • Compliance Strategy
  • Product Development
  • Verification Plans
  • Market Access Strategies
Tools & Technologies
  • Third-Party Certification Laboratories
  • UL
  • TÜV
  • CSA
  • Intertek
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