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Supplier Quality Engineer III

Boston Scientific · Arden Hills, MN

Level
Senior
Team
Quality
Travel
25%
Degree
Required
Experience asked
5+ years
Industry
Medical devices
Posted
22 days ago

The role in 30 seconds

A senior quality role at Boston Scientific (medical devices) in Arden Hills, MN. In this role, you will support SFMD products within the Electrophysiology division with a primary focus on Single-Use Devices and Capital Equipment.

They ask for
5+ years · degree required
Tools it names
Validation (IQ/OQ/PQ), Internal audits, Supplier quality
Day to day
about 25% travel · relocation help

Read from the posting. The full description is below.

How this role compares

Against 50 other live quality postings in Minnesota.

Base pay
Not listed in this posting

Typical $83k–$131k, from 30 postings that list pay.

Experience asked
Typical (5+ years)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • Root cause 59%
  • Six Sigma 43%
  • ✓ Validation (IQ/OQ/PQ) 43%
  • Lean 39%
  • ✓ Supplier quality 39%
  • FMEA 37%

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

It asks for 5+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team 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 10 people at this company and state: 9 on the team, 1 leaders, plus 1 likely hiring manager. 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.

    Write to Mackenzie → (free)
  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 25% 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 Arden Hills

12 other open roles at this site · 10 people we found on the quality team.

All 13 roles at Boston Scientific →
Full description from Boston ScientificAs posted on their careers site.Show

requirements

as well as supporting any

requirements

from the supplier’s Quality system.

  • ✓Quality record ownership requiring technical writing skillset to formally document investigations, testing and verification of effectiveness actions utilizing statistical and industry standard quality tools

Required Qualifications

  • ✓Minimums of BS degree in engineering or technical field
  • ✓Minimum of 5 years of relevant exper
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.

SUPPLIER QUALITY ENGINEER III – Electrophysiology External Operations

The External Operations organization focuses on Sourced Finished Medical Device (SFMD) at Boston Scientific and is a global, passionate team that oversees a diverse network of suppliers which manufacture finished devices for BSC distribution. The Supplier Quality Engineer III will demonstrate a primary commitment to patient safety and compliance through collaboration with cross-functional internal/external resources to continually improve our supplier’s manufacturing processes to ensure finished device quality. In this role, you will support SFMD products within the Electrophysiology division with a primary focus on Single-Use Devices and Capital Equipment.

Additionally, the Supplier Quality Engineer will support global sourcing, supplier manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects.

Work model, sponsorship, relocation

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

Function or Divisional Overview

At Boston Scientific, our products and technologies support the diagnosis and treatment of a wide range of medical conditions, with a focus on advancing less invasive care. Within the Electrophysiology (EP) portfolio, Boston Scientific develops, manufactures, and markets solutions designed to treat complex cardiac arrhythmias and enable precise, catheter-based interventions.

The EP portfolio includes technologies for cardiac mapping and navigation, radiofrequency ablation, diagnostic electrophysiology, EP recording systems, and intracardiac access and steerable sheath solutions, supporting physicians across the full EP procedure workflow. These products are designed to improve procedural efficiency, precision, and patient outcomes in the treatment of cardiac rhythm disorders.

Boston Scientific continues to invest in innovation, clinical research, and global expansion within Electrophysiology, extending access to advanced therapies across key geographies. Through ongoing portfolio development and clinical evidence generation, the EP division supports the evolution of catheter-based treatment strategies for some of the most complex and prevalent cardiac arrhythmias.

New Product Development

  • •Core team member to support product launch through execution of SFMD Plan deliverables for integration and/or onboarding of supplier and related products into BSC’s Quality System.
  • •Lead the execution of SFMD quality deliverables and collaborate with cross-functional new product development teams to onboard finished medical device suppliers.
  • •Generate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, process validations, and incoming inspection requirements.
  • •Lead and support initial on-boarding assessments, new manufacturing locations and supplier’s approved status

Sustaining Supplier Quality & Compliance

  • •Responsible for ongoing supplier qualification and performance monitoring based on supplier risk. Assess suppliers for technical, quality and manufacturing capabilities
  • •Plans and leads supplier audits to assess compliance with regulatory standards and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions
  • •Assess & drive reactive as well as proactive supplier project(s)/investigations partnering with Supplier Engineering, Commercial Sourcing, Design Assurance.
  • •Investigates & solves non-conformances due to product realization, product performance, incoming inspection, audit findings, & field failures related to supplier materials. Develop corrective action plan where necessary. Applies sound, systematic problem-solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation
  • •Supports supplier change impact assessments, process change impacts, and design change implementations for suppliers within the BSC quality system

Quality System Champion

  • •Supports Material Controls external regulatory body audits requests as required.
  • •Leads or supports Material Controls internal audit efforts.
  • •Collaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents.
  • •Identifies and advises management on potential improvements to quality systems and processes in the company.
  • •Champions 100% compliance to company policies and SOP’s.

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