Associate Supervisor, Quality Control

Reposted 23 Days Ago
Be an Early Applicant
Redmond, WA, USA
In-Office
89K-149K Annually
Junior
Healthtech
The Role
Supervise Quality Technicians across incoming, in-process, and final inspection activities to ensure compliant release of materials and finished goods. Manage daily workload, track quality/operational metrics, lead MRB disposition, support audits, maintain training and competency, and drive continuous improvement and corrective actions to meet regulatory and performance targets.
Summary Generated by Built In
Work Flexibility: Onsite

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.

  • 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.
  • 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.
  • 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

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The Company
HQ: Irvine, CA
956 Employees

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.

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