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Design Quality Assurance Engineer III - Endoscopy

Boston Scientific · Marlboro, MA

Level
Senior
Team
Quality
Travel
20%
Degree
Required
Experience asked
3+ years
Industry
Medical devices
Posted
Yesterday

The role in 30 seconds

A senior quality role at Boston Scientific (medical devices) in Marlboro, MA. 5 Whys, Is-Is Not, DMAIC and Six Sigma problem solving methodologies) to diagnose root causes, optimize processes, and ensure sustained corrective actions.

They ask for
3+ years · degree required
Tools it names
Six Sigma, Root cause, DMAIC, CAPA, Minitab, ISO 13485
Day to day
about 20% travel · relocation help

Read from the posting. The full description is below.

From the plant jobs report · week of November 2, 2026

Quality Engineer roles in Massachusetts: typical posted base $107k–$155k.

Median of the low and high ends of 55 live postings that list pay, out of 91 quality engineer openings in Massachusetts, read from manufacturers' own careers sites.

Massachusetts plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 90 other live quality postings in Massachusetts.

Base pay
Not listed in this posting

Typical $102k–$140k, from 42 postings that list pay.

Experience asked
Less than usual (3+ vs 5+)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • ✓ Root cause 63%
  • ✓ FDA / GMP 46%
  • ✓ Validation (IQ/OQ/PQ) 41%
  • ✓ CAPA 37%
  • ✓ ISO 13485 33%
  • Supplier quality 30%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for DMAIC, Minitab, which few similar roles mention. If you have it, lead with it.

It asks for 3+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Relocation help

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at Boston Scientific

    We found 3 people at this company and state: 3 in this kind of role. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

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  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • The posting says about 20% travel. Between which sites?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Boston Scientific in Marlboro

2 other open roles at this site · 3 people we found in quality roles at Boston Scientific.

Full description from Boston ScientificAs posted on their careers site.Show

Required Qualifications

  • ✓BS in Biomedical Engineering, Mechanical Engineering or related degree.
  • ✓Minimum of 3 years of medical device engineering experience.
  • ✓Detailed understanding and working knowledge of US and International medical device

requirements

including 21 CFR part 820, Medical Device Directive (MDD) / Medical Device Regulation (EU MDR), EN ISO 13485 and EN ISO 14971.

  • ✓Proven experience leading and owning CAPAs within the design environment, and proficiency in root cause analysis tools and methodologies.
  • ✓Travel approximately 10-20%.

Preferred Qualifications

  • ✓5+ years of medical device engineering experience.
  • ✓Proficiency in Minitab Statistical Analysis software or equivalent.
  • ✓Six Sigma Certification.
  • ✓Strong technical expertise in quality engineering principles, design controls, risk management, and problem-solving methodologies.
  • ✓Excellent communication, presentation, and interpersonal skills, with the ability to influence teams and leadership.
  • ✓Proven ability to lead and coach others, driving a high-performance quality culture.
  • ✓Strategic mindset with hands-on execution, balancing long-term objectives with immediate project needs.

Minimum Salary: $ 82100

Maximum Salary: $ 156000

For MA positions : It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce th

Show full description ↓

Additional Location(s): N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About this role

The Design Quality Assurance Engineer III is responsible for leading complex design-related nonconformance (NCEP) and CAPA activities across the product lifecycle. This individual will work with high-performing cross-functional development team to ensure safety, quality and compliance of our products while continuously improving their commercial value.

The position is part of the design site for the Endoscopy Division and supports activities such as NCEP/CAPA, Quality Process Improvements, and Quality Systems initiatives related to design and development.

Work mode

At Boston Scientific, we value collaboration and synergy. This hybrid role is based in Marlborough, MA and requires being on-site at least three days per week.

Relocation assistance

Relocation assistance is not available for this position at this time.

Visa sponsorship

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Your

include

  • •Leads and provides quality oversight for complex design-related NCEP/CAPA activities, ensuring timely progression through all phases while maintaining compliance with regulatory and Quality System requirements.
  • •Leverages technical knowledge to lead teams through complex investigation and problem-solving initiatives. Applies systematic approaches (e.g. 5 Whys, Is-Is Not, DMAIC and Six Sigma problem solving methodologies) to diagnose root causes, optimize processes, and ensure sustained corrective actions.
  • •Partners with cross-functional teams to develop risk-appropriate corrective and preventive actions that effectively address identified causes and support sustainable solutions.
  • •Working knowledge of Design Controls. Provide quality and compliance input to project teams for project decisions and deliverables (i.e. Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Reviews, Design V&V, Usability Testing, Process Validation and Labeling).
  • •Guides and mentors engineers, fostering a culture of learning, collaboration, and technical excellence. Provides coaching on quality engineering methodologies and problem-solving techniques.
  • •Acts as the primary voice for quality within cross-functional teams, influencing project direction and ensuring adherence to regulatory requirements, internal procedures, and best quality practices.
  • •Identifies and implements best-in-class practices for the department. Proactively assesses opportunities for improvements or enhancement to quality systems and processes in the company.
  • •Supports internal and external regulatory audits as required.

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