Stryker is seeking an Associate Quality Manager, Stability to support our Stryker Sage Medical division in Cary, IL to provide leadership for the Stability function, overseeing team performance, processes, and procedures while advancing quality excellence across the product lifecycle. This role ensures compliance with U.S. and international regulatory requirements and supports quality activities from product development through commercial manufacturing and post‑market surveillance.
What you will do:
Lead and continuously advance a best‑in‑class Stability program, ensuring compliance with global regulatory requirements (ICH, FDA, ISO) and inspection readiness at all times
Provide strategic and operational oversight of stability study design, execution, monitoring, and reporting, including support for regulatory submissions and product quality reviews
Establish, maintain, and improve stability policies, procedures, systems, and documentation to drive consistency, scalability, and data integrity
Analyze stability data and trends to proactively identify risks, mitigate issues, and drive continuous quality and product lifecycle improvements
Plan, prioritize, and oversee team deliverables; monitor progress and assess results to ensure alignment with organizational and business objectives
Partner cross‑functionally with Quality, Regulatory, R&D, Manufacturing, and Supply Chain to ensure alignment, effective decision‑making, and timely outcomes
Build and lead high‑performing teams by setting clear goals, KPIs, and performance expectations; coach, develop, and address performance to maximize engagement and results
Recruit, onboard, and retain top talent while fostering a culture of accountability, collaboration, and continuous improvement
What you need:
Required
Bachelor’s degree in a Science, Engineering, or related
Minimum of 6+ years’ experience - supporting Pharmaceutical Quality Control and Quality Assurance functions, with demonstrated success driving quality improvements through data and quality system improvements.
Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.
Proven ability to analyze complex data sets using sound mathematical and statistical principles to inform decisions and drive effective, executable actions
Preferred
3+ supervisory experience with demonstrated people‑leadership exposure, including mentoring, training, and developing high‑performing direct and indirect reports
Quality Engineer (ASQ CQE) Certification preferred.
Demonstrated ability to effectively communicate and influence stakeholders at all levels of the organization, with proven success working in cross‑functional team environments
United States of America Pay Ranges:
US10: $112,900 - $188,100 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.
Skills Required
- Bachelor's degree in a Science, Engineering, or related field
- Minimum of 6+ years' experience in Pharmaceutical Quality Control and Assurance
- Deep expertise in pharmaceutical stability testing
- Proven ability to analyze complex data sets
- 3+ years supervisory experience (preferred)
- Quality Engineer (ASQ CQE) Certification (preferred)
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.
