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Director Stryker Medical Devices Jobs (NOW HIRING)

Advanced Quality Engineer

Tempe, AZ · Hybrid

$76K - $122K/yr

... medical devices is safe, effective, and compliant with industry practices. Working closely with R&D ... Stryker is an EO employer - M/F/Veteran/Disability. Stryker Corporation will not discharge or in ...

... medical devices. This position contributes to packaging design, validation, and regulatory ... None Stryker Corporation is an equal opportunity employer. Qualified applicants will receive ...

... medical devices. This position contributes to packaging design, validation, and regulatory ... None Stryker Corporation is an equal opportunity employer. Qualified applicants will receive ...

Design, develop, and verify components and subsystems for medical devices with minimal supervision ... Stryker is an EO employer - M/F/Veteran/Disability. Stryker Corporation will not discharge or in ...

Hybrid At Stryker, we're committed to improving healthcare through cutting-edge medical ... Design, develop, and verify components and subsystems for medical devices with minimal supervision.

Preferred: * 5+ years' experience in sales. * 2+ years' experience in medical devices/disposables ... Travel Percentage: 50% Stryker Corporation is an equal opportunity employer. Qualified applicants ...

Preferred: * 5+ years' experience in sales. * 2+ years' experience in medical devices/disposables ... Travel Percentage: 50% Stryker Corporation is an equal opportunity employer. Qualified applicants ...

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Director Stryker Medical Devices information

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$13K

$232.4K

$357K

How much do director stryker medical devices jobs pay per year?

As of Aug 14, 2026, the average yearly pay for director stryker medical devices in the United States is $232,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $198,000.00 and $284,500.00 per year, depending on experience, location, and employer.

What does a director at Stryker Medical Devices do?

A Director at Stryker Medical Devices is a senior leader responsible for overseeing business operations, strategy, and team management within a specific division or product line. They focus on driving growth, ensuring compliance with industry regulations, and fostering innovation in medical device development. Directors collaborate with cross-functional teams, manage budgets, and build relationships with key stakeholders to achieve organizational goals. Their role is critical in maintaining Stryker’s reputation for quality and advancing healthcare solutions.

How does a director at Stryker Medical Devices typically collaborate with cross-functional teams to drive product innovation?

As a Director at Stryker Medical Devices, you will regularly work with cross-functional teams, including R&D, regulatory affairs, marketing, and manufacturing, to ensure successful product development and launch. Collaboration often involves leading strategy meetings, aligning project goals, and resolving challenges that arise during the product lifecycle. Effective communication and leadership are essential, as you guide teams through decision-making processes and ensure compliance with industry standards. This role provides opportunities to influence the company's innovation pipeline and shape product strategies in a highly regulated, fast-paced environment.

What is the difference between Director Stryker Medical Devices vs Product Manager Stryker Medical Devices?

AspectDirector Stryker Medical DevicesProduct Manager Stryker Medical Devices
ResponsibilitiesOversees multiple product lines, strategic planning, and team leadershipManages specific product lifecycle, market research, and product development
Required CredentialsTypically requires a bachelor’s degree, MBA preferred, extensive industry experienceBachelor’s degree, experience in product management, technical background often preferred
Work EnvironmentCorporate office, cross-functional teams, strategic meetingsProduct development teams, marketing, sales, and customer feedback sessions

The main difference between a Director Stryker Medical Devices and a Product Manager Stryker Medical Devices lies in scope and responsibilities. The director oversees multiple products and strategic initiatives, while the product manager focuses on individual products' lifecycle and market success. Both roles require relevant industry experience and technical knowledge, but the director's role is more leadership and strategy-oriented.

What are the key skills and qualifications needed to thrive as a director at Stryker Medical Devices, and why are they important?

To thrive as a Director at Stryker Medical Devices, you need extensive experience in medical device management, a strong background in business strategy, and often an advanced degree in engineering, life sciences, or business. Familiarity with regulatory compliance (FDA, ISO), ERP systems, and project management tools is typically required, along with relevant certifications such as PMP or Six Sigma. Exceptional leadership, communication, and decision-making skills help drive cross-functional teams and foster innovation. These qualifications and skills are crucial for ensuring product quality, regulatory adherence, and sustained organizational growth in a highly competitive industry.
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Infographic showing various Director Stryker Medical Devices job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $232,369 per year, or $111.7 per hour.

Advanced Quality Engineer

Stryker

Tempe, AZ • Hybrid

$76K - $122K/yr

Full-time

Posted 9 days ago


Job description

Work Flexibility: Hybrid or Onsite

Stryker is hiring an Engineer, Advanced Quality Engineering for our Sustainability Solutions team supporting our reprocessing product line. You will be a key member of the new product development team ensuring the implementation of cutting-edge technology for medical devices is safe, effective, and compliant with industry practices. Working closely with R&D, Marketing, Advanced Operations, and Regulatory Affairs team members, you will be in a fast-paced environment with opportunities to win for yourself, the company, and patients around the world. This position is a hybrid between a traditional R&D Engineer and a traditional Quality Engineer.

Workplace Flexibility: Candidate must reside within a commutable distance to Tempe, AZ and is expected to be onsite 3+ days/week at the facility and is not eligible to be fully remote.

What you will do:

  • Represents Quality Assurance on New Product Development (NPD) cross-functional teams, collaborating with R&D, Regulatory Affairs, Advanced Operations, and Marketing to meet product development metrics.

  • Supports Risk Management activities, including creating and implementing Risk Management Files, identifying hazards, and ensuring compliance with corporate and local design control procedures.

  • Plans, designs, and implements inspection, testing, and evaluation methods to ensure product and production reliability, applying advanced statistical techniques for test sample size determinations.

  • Supports Design Reviews to ensure design and process robustness, compliance with applicable regulations (e.g., QSR, ISO 13485), and proper risk analysis for new medical devices.

  • Plans, performs, and reviews engineering risk analyses, test methods, and process improvements to enhance product quality and manufacturing efficiency.

  • May interact with customers to address product quality concerns, provide training on quality assurance and GMP topics, and support continuous improvement initiatives.

What you will need:

Required:

  • Bachelor's degree in Mechanical, Electrical, Chemical, Material Science, Biomedical Engineering or related Science or engineering discipline

Preferred:

  • Experience in data collection, data analysis, and scientific method.

  • Experience with Quality Concepts such as Risk Management, CAPA, Audits, Statistics.

  • Previous medical device industry experience preferred

  • Understanding of US and International Medical Device Regulations, including ISO 13485, GDP, GMP.

$76,500 - $122,000 USD Annual

Travel Percentage: 10%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.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.