Stryker is hiring a Senior Manager, Quality Operations for our Emergency Care division. This is an onsite role based in Redmond, Washington.
As the Senior Manager, Quality Operations, you will lead the team responsible for quality process execution, issue resolution, performance monitoring, and continuous improvement initiatives. You will partner across functions to ensure quality systems remain effective, compliant, and aligned with business objectives while supporting product quality and patient safety.
This position is responsible for leading quality systems and process excellence activities, managing quality performance across the organization, supporting regulatory compliance, and developing teams that ensure consistent execution of quality processes and continuous improvement initiatives.
What You Will Do
Lead day-to-day quality system activities, ensuring quality issues, investigations, and corrective actions are evaluated, documented, and resolved in a timely manner.
Establish and monitor quality performance metrics, key performance indicators, and reporting processes to identify trends and drive continuous improvement.
Manage product quality, safety, complaint, and corrective action processes, ensuring compliance with applicable regulatory and quality requirements.
Develop and implement quality process improvements, standardization initiatives, and operational strategies to improve efficiency and consistency across the organization.
Partner with Quality Assurance, Research & Development, Manufacturing, Supply Chain, Commercial, and Finance teams to support business and quality objectives.
Represent quality systems and processes during internal, external, regulatory, and third-party audits, ensuring audit readiness and effective follow-up actions.
Develop annual budgets, forecasts, resource plans, and departmental objectives to support organizational priorities.
Recruit, develop, coach, and manage team members, establishing performance goals and supporting employee development and succession planning.
What You Need
Required
Bachelor’s degree in Engineering, Life Sciences, Quality, Manufacturing, or a related discipline.
Minimum 10 years of experience in Quality, Quality Systems, Manufacturing Quality, Regulatory Affairs, or a related regulated industry function.
Minimum 4 years of people leadership experience, including performance management and employee development responsibilities.
Experience working within a regulated environment governed by FDA, ISO, or other international quality and regulatory requirements.
Experience managing quality systems, complaint investigations, corrective and preventive action processes, or product quality programs.
Preferred
Master’s degree in Engineering, Science, Quality, Business, or a related field.
Experience applying Lean, Six Sigma, or other continuous improvement methodologies.
Experience with enterprise resource planning systems, including SAP, Oracle, or JD Edwards.
- US15: $155,900 - $259,800 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.
Skills Required
- Bachelor's degree in Engineering, Life Sciences, Quality, Manufacturing, or related discipline.
- Minimum 10 years of experience in Quality, Quality Systems, Manufacturing Quality, Regulatory Affairs, or related regulated industry function.
- Minimum 4 years of people leadership experience, including performance management and employee development.
- Experience working within a regulated environment governed by FDA, ISO, or other international quality and regulatory requirements.
- Experience managing quality systems, complaint investigations, corrective and preventive action (CAPA) processes, or product quality programs.
- Master's degree in Engineering, Science, Quality, Business, or related field.
- Experience applying Lean, Six Sigma, or other continuous improvement methodologies.
- Experience with enterprise resource planning systems, including SAP, Oracle, or JD Edwards.
Inari Medical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.
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Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
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Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
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Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.
Inari Medical Insights
What We Do
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.
