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Staff Engineer, Quality

Stryker

Waltham, MAJob$107–179K/yrSeen 2w agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$107–179K/yr
Location
Waltham, MA
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Stryker’s Amplitude Vascular Systems team in Waltham, Massachusetts seeks a Staff Quality Engineer to support manufacturing operations, supplier quality, and process performance for existing and new products, ensuring compliance with quality standards, regulatory requirements, and customer expectations.

Skills & qualifications

RequiredNice to have

Skills

Manufacturing ReadinessProduct TransferProcess ImprovementInvestigationCorrective and Preventive ActionsMaterial Review BoardChange ManagementProcess ValidationEquipment QualificationMeasurement System AnalysisAuditsSupplier Quality Performance

Qualifications

Bachelor's Degree in Engineering, Quality, Life Sciences or Related Technical Discipline4 Years Experience in Quality Engineering, Quality Assurance or Related Quality Focused Role Supporting Manufacturing Operations Within a Regulated EnvironmentExperience Working Within a Regulated Manufacturing EnvironmentExperience in Medical Device ManufacturingTraining or Certification in Lean, Lean Six Sigma, or Continuous Improvement MethodologiesExperience With Process Capability Analysis, Statistical Sampling Plans, and Gauge Repeatability and Reproducibility StudiesWorking Knowledge of ISO 13485, Good Manufacturing Practices, CAPA, Risk Management, Audits, and Statistical Quality Methods

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Join Stryker’s Amplitude Vascular Systems (AVS) team in Waltham , Massachusetts as a Staff Quality Engineer . In this role, you will support manufacturing operations, supplier quality, and process performance across both existing and new products. Working closely with operations, engineering, suppliers, and cross-functional partners, you will help ensure products and manufacturing processes meet quality standards, regulatory requirements, and customer expectations.

This role offers a unique opportunity to support a newly integrated business preparing for commercial launch. As the site's primary Quality Engineer, you will play a key role in helping to establish quality metrics, drive process improvements, support manufacturing readiness activities, and enhance long-term quality and operational performance.

What You Will Do

  • Support manufacturing readiness, product transfer activities, and the transition from development to sustaining operations.

  • Identify and implement process improvements that enhance product quality, manufacturing efficiency, inspection effectiveness, and compliance.

  • Lead investigations of internal and supplier nonconformances, ensuring timely resolution and closure.

  • Own Corrective and Preventive Actions (CAPAs), using root cause analysis to identify issues and implement sustainable solutions.

  • Review and disposition nonconforming product through Material Review Board activities and containment actions.

  • Partner with operations and cross-functional teams to resolve quality issues and maintain process compliance.

  • Evaluate manufacturing and quality performance metrics, identify trends, and drive continuous improvement initiatives.

  • Support manufacturing complaints, product field actions, and quality-related investigations.

  • Review and approve change management activities, challenge effectiveness, and verify implementation of quality controls.

  • Support process validation, equipment qualification, measurement system analysis, audits, and supplier quality performance activities.

What You Will Need

Required Qualifications

  • Minimum bachelor's degree in Engineering, Quality, Life Sciences, or a related technical discipline.

  • Minimum 4 years of experience in Quality Engineering, Quality Assurance, or a related quality-focused role supporting manufacturing operations within a regulated environment.

  • Experience working within a regulated manufacturing environment.

Preferred Qualifications

  • Experience in medical device manufacturing.

  • Training or certification in Lean, Lean Six Sigma, or continuous improvement methodologies.

  • Experience with process capability analysis, statistical sampling plans, and gauge repeatability and reproducibility (Gage R&R) studies.

  • Working knowledge of ISO 13485, Good Manufacturing Practices (GMP), CAPA, risk management, audits, and statistical quality methods

US20 : $107,200 - $178,600 USD Annual

View the U.S. work location and transparency guide (https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) to find the pay range for your location.

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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