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Staff Design Quality Engineer

Stryker

Waltham, MA · HybridJob$93–155K/yrSeen 3 days agoSeen in employer's feed 3 days ago

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At a glance

Compensation
$93–155K/yr
Location
Waltham, MAHybrid
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Staff Design Quality Engineer supports new product development and quality activities across the medical device product lifecycle. The role partners with Research & Development, Regulatory Affairs, Manufacturing, Supplier Quality, and Operations on design controls, risk management, verification and validation, design transfer, and Quality Management System compliance. It is hybrid, with several onsite days per week and a requirement to reside within commuting distance of Waltham, Massachusetts.

Skills & qualifications

RequiredNice to have

Skills

New Product DevelopmentDesign ControlsFDA 21 CFR Part 820ISO 13485ISO 14971Corrective and Preventive ActionChange ManagementProcess ValidationElectronic Quality Management SystemsClass II and III Medical DevicesEuropean Union Medical Device RegulationMedical Device Single Audit ProgramStatistical AnalysisQuality Improvement MethodologiesSupplier Quality ManagementAuditingSoftware ValidationComputerized System Validation

Qualifications

Bachelor's in Engineering or Related4+ Years Quality Engineering ExperienceCertified Quality Engineer or Comparable

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Staff Design Quality Engineer

Waltham – MA

Join Stryker as a Staff Design Quality Engineer supporting new product development and quality activities throughout the medical device product lifecycle. In this role, you will partner with Research & Development, Regulatory Affairs, Manufacturing, Supplier Quality, and Operations to support design controls, risk management, product verification and validation, design transfer, and Quality Management System compliance in a regulated medical device environment.

Work Flexibility:

Hybrid: candidates must reside within commuting distance of Waltham – MA and be able to work onsite several days per week.

What you will do

  • Represent Quality Engineering on cross-functional new product development teams, providing quality and regulatory guidance throughout the product lifecycle.

  • Review and approve design control documentation, including design plans, user needs, design inputs and outputs, verification and validation protocols and reports, design reviews, and Design History File documentation.

  • Apply risk management principles in accordance with ISO 14971 and participate in design reviews and product risk assessments.

  • Support verification, validation, process validation, and design transfer activities to ensure established requirements and acceptance criteria are addressed.

  • Evaluate product requirements, specifications, engineering changes, and manufacturing changes for quality and regulatory impact.

  • Investigate product and development issues using root cause analysis and support corrective and preventive actions, nonconformances, change control, and complaint investigations.

  • Maintain quality documentation and records in accordance with ISO 13485, FDA 21 CFR Part 820, and applicable global medical device requirements.

  • Support internal and regulatory audits, supplier quality activities, regulatory submissions, and updates to quality procedures, work instructions, and quality system requirements.

What you will need

Required

  • Bachelor’s degree in Engineering, Life Sciences, Biomedical Engineering, Manufacturing Engineering, or a related technical discipline.

  • Minimum 4 years of experience in Quality Engineering, Quality Assurance, or a related position within the medical device industry.

  • Experience supporting new product development, including design control activities.

  • Working knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, design controls, corrective and preventive action, change management, and process validation.

  • Experience using electronic Quality Management Systems.

Preferred

  • Certified Quality Engineer (CQE) certification or a comparable quality certification.

  • Experience with Class II and/or Class III medical devices, including global requirements such as the European Union Medical Device Regulation and Medical Device Single Audit Program.

  • Experience with statistical analysis, quality improvement methodologies, supplier quality management, auditing, software validation, or computerized system validation.

US20 : $93,200 - $155,400 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.

How this job compares

Set against the 888 open Quality Engineering jobs on Olive Jobs, counted October 27, 2026.

Pay
  • This posting$93–155K/yr
  • Massachusetts median$117–181K/yr24 salary ranges
  • US median$115–175K/yr488 salary ranges

This range's midpoint, $124K, is 14% below the Massachusetts median midpoint ($145K) — in the lowest quarter of Quality Engineering salary ranges in Massachusetts.

Openings
Olive Jobs lists 33 open Quality Engineering jobs in Massachusetts and 888 across the US. 3% of them nationwide are listed as remote or flexible.
Hiring the most in Massachusetts
Experience
This posting asks for at least 4 years of experience; Quality Engineering postings that state a minimum ask for 5 years at the median (630 postings).
Education
This posting asks for a bachelor's degree; 403 of the 888 open Quality Engineering jobs (45%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on October 27, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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