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Director Stryker Medical Devices Jobs in Bothell, WA

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

Manufacturing Supervisor

Redmond, WA · On-site

$89K - $148K/yr

Onsite Join a manufacturing team responsible for the production of Class III medical devices in a ... Direct daily production activities by allocating people, equipment, materials, and systems to ...

Stryker

OnSite Specialist - Silverdale, WA

Seattle, WA · On-site

$24.82 - $33.58/hr

Is responsible for trouble-shooting and maintaining Stryker equipment and or other related devices ... Adheres to all Stryker and medical facility policies, standards and procedures. Analyze and resolve ...

Stryker

OnSite Specialist - Silverdale, WA

Silverdale, WA · On-site

$24.82 - $33.58/hr

... Stryker equipment and or other related devices. • Works with surgeons, O.R. personnel, central ... by Stryker and the medical facility. • Adhere to (HIPAA) and other related patient ...

Eden Health

Hospice Medical Director

Everett, WA · On-site

The Medical Director works to establish relationships with the medical community in order to ... Home Visits * On Call * Prescribes Medications and Other Regulated Medical Devices * Doctorate in ...

Concentra

Medical Assistant

Tukwila, WA

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

New

Concentra

Medical Assistant

Seattle, WA · On-site

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Tukwila, WA

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

New

Concentra

Medical Assistant

Seattle, WA · On-site

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Seattle, WA

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Seattle, WA

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Seattle, WA

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Seattle, WA

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Seattle, WA · On-site

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Concentra

Medical Assistant

Seattle, WA · On-site

$20.25 - $26/hr

... under direct supervision of the treating clinician as well as supports in other areas of the ... Maintain and operate all medical devices and equipment, including calibration and record keeping in ...

Stryker Group

Manufacturing Supervisor

Redmond, WA · On-site

$89.40 - $148.90/hr

Join a manufacturing team responsible for the production of Class III medical devices in a ... Direct daily production activities by allocating people, equipment, materials, and systems to ...

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All JobsStryker Medical Devices JobsDirector Stryker Medical Devices JobsDirector Stryker Medical Devices Jobs in Bothell, WA

Director Stryker Medical Devices information

See Bothell, WA salary details

$14.5K

$259.8K

$399.1K

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

As of Aug 28, 2026, the average yearly pay for director stryker medical devices in Bothell, WA is $259,762.00, according to ZipRecruiter salary data. Most workers in this role earn between $221,300.00 and $318,000.00 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 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.

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 popular job titles related to Director Stryker Medical Devices jobs in Bothell, WA?

For Director Stryker Medical Devices jobs in Bothell, WA, the most frequently searched job titles are:

What job categories do people searching Director Stryker Medical Devices jobs in Bothell, WA look for?

The top searched job categories for Director Stryker Medical Devices jobs in Bothell, WA are:

Director Stryker Medical Devices jobs near you
Infographic showing various Director Stryker Medical Devices job openings in Bothell, WA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $259,762 per year, or $124.9 per hour.

Senior Staff Medical Writer (Remote)

Stryker

Seattle, WA • On-site, Remote

$143K - $238K/yr

Full-time

Posted 10 days ago

Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

130th of 495 rated machine equipment manufacturers

Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

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.

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