Join Stryker as an Associate Supervisor, Quality Control in Redmond, WA supporting Emergency Care! In this role, you will oversee critical quality control activities that ensure compliant release of materials and finished goods while maintaining inspection effectiveness and operational flow. This position provides direct leadership of Quality Technicians and accountability for execution across incoming, in-process, and final quality activities.
Work flexibility: Onsite. Occasional off-hours support, while infrequent, may be needed to ensure consistent quality and operational continuity
What you will do
Supervise Quality Technicians performing Incoming Quality Assurance (IQA), Finished Goods Acceptance (QAR), and non-conformance review activities, ensuring adherence to defined procedures and regulatory requirements
Assign daily work, balance workload, and monitor throughput to maintain on-time inspection and material release performance targets
Establish, track, and report key quality and operational metrics (e.g., inspection cycle time, backlog, defect rates) and implement corrective actions when targets are not met
Oversee inspection methods, sampling plans, and test procedures for incoming components and finished goods, ensuring alignment with specifications and standards
Lead Material Review Board (MRB) activities, including evaluation and disposition of non-conforming material within defined timelines
Support internal and external audits, including preparation of documentation, responses to findings, and execution of corrective actions
Develop and maintain team training plans; ensure all personnel meet required training completion and competency requirements
Drive process improvements using structured problem-solving methods, including root cause analysis and implementation of corrective and preventive actions
Leadership Expectations
Lead with accountability while building a positive, engaged team environment
Drive productivity and operational performance through clear expectations and hands-on support
Champion a continuous improvement mindset across the team and processes
What you will need
Required Qualifications:
Associate degree
Minimum 2 years of supervisory or team leadership experience
Minimum 2 years of experience in Quality within medical devices or other regulated industry
Preferred Qualifications:
Bachelor’s degree strongly preferred
Minimum 5 years of experience in Quality within medical devices or regulated manufacturing environment
Experience supporting FDA-regulated manufacturing operations or equivalent compliance frameworks
Experience with inspection methods, sampling plans, and measurement system evaluation
Prior non-exempt labor supervisory experience with a focus on inspection or non-conforming material disposition.
US15: $89,400 - $148,900 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
Travel Percentage: 0%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
- Associate degree
- Minimum 2 years supervisory or team leadership experience
- Minimum 2 years of experience in Quality within medical devices or other regulated industry
- Onsite work in Redmond, WA; occasional off-hours support as needed
- Bachelor's degree
- Minimum 5 years of experience in Quality within medical devices or regulated manufacturing environment
- Experience supporting FDA-regulated manufacturing operations or equivalent compliance frameworks
- Experience with inspection methods, sampling plans, and measurement system evaluation
- Prior non-exempt labor supervisory experience focused on inspection or non-conforming material disposition
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.







