Senior Quality Assurance Manager - Surgical Support & Post Market

Stryker Corporation; San Jose (CA); Hybrid; USD 176,000 - 294,000; Full time

Job summary

Stryker Corporation in San Jose, CA is seeking a Senior Quality Assurance Manager for Surgical Support & Post Market to lead quality across the Endoscopy business. You will drive regulatory compliance, risk management, and data-driven improvements while partnering with R&D, Operations, Regulatory Affairs, and Commercial teams.

You will oversee a high-performing team, guide post-market surveillance, and shape quality strategies for product lifecycle management, customer satisfaction, and safety.

Qualifications

• Bachelor's degree in Engineering, Science, or related technical discipline.
• Advanced degree (MBA, MS, or equivalent) preferred.
• Minimum 10+ years in a regulated manufacturing environment (medical device, pharmaceutical, biomedical, or automotive).
• Minimum 4+ years of people leadership experience.

Responsibilities

• Lead quality assurance support for legacy surgical device portfolios, overseeing new product development, post-market quality, and lifecycle management across the Endoscopy business.
• Partner with cross-functional leaders to define quality strategy and drive continuous improvement initiatives.
• Provide strategic direction for post-market surveillance and customer-focused quality initiatives.

Skills

Quality Assurance

Regulatory compliance

Team leadership

Quality systems

Root Cause Analysis

FMEA

SPC

CAPA

Six Sigma

Cross-functional leadership

Education

Bachelor's degree in Engineering/Science

Advanced degree preferred (MBA/MS)

Job description

## Senior Quality Assurance Manager - Surgical Support & Post MarketApplylocations: San Jose, Californiatime type: Full timeposted on: Posted Todayjob requisition id: R569883Work Flexibility: Hybrid or Onsite**Stryker** is hiring an **Senior Quality Assurance Manager - Surgical Support & Post Market** in **San Jose, CA** supporting our **Endoscopy** division, who will provide strategic leadership for quality activities across the Endoscopy business, supporting both product lifecycle management and post-market quality performance. This role is responsible for driving quality excellence, regulatory compliance, customer-focused outcomes, and continuous improvement initiatives while partnering closely with cross-functional leaders across R&D, Operations, Regulatory Affairs, and Commercial teams. The Senior Manager will lead a high-performing team, leverage quality and reliability data to influence business decisions, and ensure the effective execution of quality strategies that support product performance, patient safety, and organizational objectives.**What you will do:*** Lead Quality Assurance support for legacy surgical device portfolios, overseeing new product development, post-market quality, and lifecycle management across the Endoscopy business.* Partner with cross-functional leaders to define quality strategy, establish key performance metrics, and drive continuous improvement initiatives that enhance product quality, reliability, and customer satisfaction.* Provide strategic direction for post-market surveillance and customer-focused quality initiatives, leveraging data-driven insights to influence business decisions and risk mitigation activities.* Monitor, analyze, and communicate product quality and reliability trends to senior leadership, driving proactive actions and executive-level reviews to ensure sustained product performance.* Lead resolution of complex quality issues by chairing cross-functional review boards, overseeing engineering change assessments, and ensuring robust risk analysis and verification activities.* Ensure compliance with global regulatory and quality system requirements, including FDA and international standards, while supporting regulatory inspections and external audits.* Evaluate and improve quality system processes, driving corrective and preventive actions and fostering a culture of operational excellence and continuous improvement.* Build, lead, and develop high-performing teams through talent acquisition, coaching, performance management, workforce planning, and accountability for achieving organizational objectives.**What you need****Required*** Bachelor's degree in Engineering, Science, or a related technical discipline.* Minimum of 10+ of experience in a regulated manufacturing environment (medical device, pharmaceutical, biomedical, or automotive),* Minimum of 4+ years of people leadership experience, including team development, performance management, and talent acquisition.* Experience supporting product quality throughout the product lifecycle, including post-market quality, customer quality, quality engineering, and/or manufacturing quality.* Demonstrated application of quality and risk management tools, including Root Cause Analysis, FMEA, Statistical Process Control (SPC), CAPA, and/or Six Sigma methodologies.* Experience supporting compliance with Quality Systems and regulatory requirements, including FDA regulations, audits, inspections, and/or international quality standards.* Experience leading cross-functional quality initiatives, process improvements, or quality system enhancements across multiple functions, products, or sites.**Preferred*** Advanced degree (MBA, MS, or equivalent) and/or ASQ Quality Engineer certification preferred.$176,300 - $293,700 USD AnnualTravel Percentage: 20%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.