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Senior Quality Engineer, New Product Introduction

Stryker

Irvine, CAJob$89–149K/yrSeen 1w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
$89–149K/yr
Location
Irvine, CA
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Senior Quality Engineer supports the introduction and transfer of new medical devices and manufacturing processes. The role provides quality engineering support across risk management, validation, inspection, supplier quality, and design transfer, partnering with Engineering, Manufacturing, Design Assurance, and Quality teams. It requires a bachelor’s degree and at least two years of relevant experience in a regulated manufacturing environment.

Skills & qualifications

RequiredNice to have

Skills

Risk ManagementProcess ControlsRegulated ManufacturingNew Product IntroductionMedical Device ManufacturingISO 13485Good Manufacturing PracticesGood Documentation PracticesLean Six SigmaPFMEAMeasurement System AnalysisProcess CapabilityStatistical SamplingDMAICSupplier QualificationSupplier Quality

Qualifications

Bachelor's in Engineering or Related Technical Discipline2+ Years Quality or Technical ExperienceCertified Quality Engineer or EquivalentQuality Engineering Coursework or Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Senior Quality Engineer, New Product Introduction

Irvine, CA

Join Stryker’s Quality Engineering team supporting the introduction and transfer of new medical devices and manufacturing processes. In this role, you will provide quality engineering support across risk management, validation, inspection, supplier quality, and design transfer activities while partnering with Engineering, Manufacturing, Design Assurance, and Quality teams.

What you will do

  • Support new product and process introductions by executing and documenting quality engineering activities throughout design transfer and product launch.

  • Apply risk management principles to process risk assessments, risk mitigation, process controls, and Process Failure Mode and Effects Analysis (PFMEA) in accordance with ISO 14971.

  • Develop inspection strategies, sampling plans, First Article Inspection approaches, and Measurement System Analysis (MSA) strategies to support repeatable and scalable manufacturing processes.

  • Support the development, execution, review, and approval of process validation protocols and reports, including sterilization validation activities when applicable.

  • Apply statistical methods and quality engineering tools to evaluate process capability, identify risks, investigate nonconformances, and support corrective and preventive actions.

  • Support Design for Manufacturing and Assembly through process design, inspection optimization, tooling and fixture development, and production specification development.

  • Execute supplier quality activities, including supplier qualification, validation, Production Part Approval Process (PPAP), supplier certification, and Quality Agreements.

  • Partner with cross-functional teams during design reviews and design transfer activities, documenting quality deliverables and transferring product and process knowledge to manufacturing and Quality Engineering teams.

What you will need

Required

  • Bachelor’s degree in Engineering or a related technical discipline.

  • Minimum 2 years of experience in quality, engineering or technical discipline

  • Experience in a regulated manufacturing environment.

  • Experience with risk management and process controls.

Preferred

  • Experience in new product or new process introduction.

  • Certified Quality Engineer (CQE) certification or equivalent quality engineering coursework or experience.

  • Experience with medical device manufacturing and quality requirements, including ISO 13485, Good Manufacturing Practices, and Good Documentation Practices.

  • Lean Six Sigma training and experience with quality and statistical tools such as PFMEA, MSA, process capability, statistical sampling, and DMAIC.

  • Experience with supplier qualification and supplier quality activities supporting new product introduction and manufacturing.

$89,400 - $148,900 USD Annual

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

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.

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