Top 4 Sr quality engineer Jobs in New Bedford Ma

Sr Quality Engineer
Morgan Advanced Materials —New Bedford, MA
- Full-time
- Engineering
- Travel
- Mentoring
Senior Engineer, Central Quality & Quality Control | Titleist
Acushnet Golf —New Bedford, MA
- $107,896 - $134,765 a year
- Full-time
- Management
- Engineering
- Driver's License
- Health savings account
- Flexible spending account
Senior Design Quality Engineer
Katalyst Healthcares & Life Sciences —Raynham, MA
- Contract
- 5 years
- Engineering
- Senior level
Quick Apply
Senior Quality Assurance Engineer
TherapyNotes.com —United States
- $95,000 - $125,000 a year
- Full-time
- Remote
- Computer Science
- 5 years
- Bachelor of Science
- Profit sharing
- Disability insurance
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Sr Quality Engineer

Morgan Advanced Materials -
New Bedford, MA

Apply Now

Job Details

Full-time

Qualifications

Statistics
Defect resolution root cause analysis
Quality control statistical data analysis
Preventive action implementation
Production deviation management
Corrective and preventive actions (CAPA)
Bachelor's degree in engineering
Production validation processes
Root cause analysis
Statistical analysis tools
Customer complaint resolution

Full Job Description

Overview:

Morgan Advanced Materials is a business rich in history and innovation. Founded in the UK in 1856, we have grown into a global organisation with 70 sites in 18 countries. Our model to serve our customers where they need us has led to a diversified product range using our unparalleled expertise in ceramic and carbon materials, which we exploit to solve difficult problems for our customers across a diverse range of markets.

We are a purpose driven organisation. Our purpose is to use advanced materials to make the world more sustainable and to improve the quality of life. We deliver on that purpose through the products that we make, and the way that we make them.

The Technical Ceramics business of Morgan Advanced Materials engineers high performance functional and structural ceramic materials, components and sub-assemblies to address customer-specific technical challenges.

Key Figures: Revenue £1,100.7m (2024), ~8,000 employees, manufacturing in 20+ countries, and a global customer portfolio. A UK PLC with head office located in Windsor, Berkshire UK. Listed on London Stock Exchange; Member of the FTSE 250 Index.

Responsibilities:

We make complex products where quality isn’t a box to tick — it’s the difference between “works perfectly” and “don’t ship it.”

As our Senior Quality Engineer, you’ll be the person who keeps processes tight, problems owned, and customers confident. You’ll sit right at the crossroads of manufacturing, engineering, and customer quality — and you’ll have the authority (and expectation) to drive real change.

This role suits someone who’s been around the block in aerospace and/or medical manufacturing, knows how things should work, and isn’t afraid to roll up their sleeves when they don’t.

The role

You’ll own product and process quality across manufacturing operations. That means leading complex investigations, running CAPAs that actually stick, working directly with customers and auditors, and keeping the Quality Management System doing what it’s meant to do — not just looking good on paper.

Some days you’ll be deep in data and root cause. Other days you’ll be on the floor, in audits, or leading cross‑functional problem‑solving sessions. No two days are the same — and that’s the point.

Key responsibilities

Lead investigations into non‑conformances, escapes, and customer complaints using structured problem‑solving methods
Own CAPAs end‑to‑end — from root cause to verified effectiveness
Analyze scrap, yield, and defect trends and turn data into action
Partner with Operations and Engineering to improve capability, reduce variation, and boost first‑pass yield
Act as the main quality contact for customers, including SCARs, audits, and technical discussions
Support and lead internal, customer, and third‑party audits (ISO 13485, AS9100, and customer requirements)
Maintain and improve core quality processes like MRB, NCMR, RMA, PFMEA, and control plans
Lead or approve validation activities (IQ, OQ, PQ) for processes and equipment
Use SPC, DOE, and capability analysis to drive data‑based decisions
Support supplier quality activities and improve measurement systems (MSA, GR&R, calibration)
Mentor other Quality Engineers and lead cross‑functional teams — without needing direct authority to get results

Qualifications:

What you’ll bring

Bachelor’s degree in Engineering (Mechanical, Electrical, Chemical, or similar)
5–10+ years of hands‑on manufacturing quality engineering experience
Background in aerospace and/or medical device manufacturing
Strong working knowledge of:
- CAPA, MRB, NCMR, and RMA processes
- Root cause methodologies (8D, DMAIC, etc.)
- Statistical tools (SPC, DOE, Minitab or equivalent)
- Process validation (IQ/OQ/PQ)
Experience working within ISO 13485 and/or AS9100 quality systems
Confidence working directly with customers, auditors, and regulators
A practical mindset — you know when to be thorough and when to be decisive

Nice to have

ASQ‑CQE certification
Experience improving yield and reducing scrap in high‑mix manufacturing
Prior mentoring or technical leadership experience

Other requirements (the fine print, but important)

This role involves Controlled Unclassified Information (CUI) subject to ITAR, EAR, and NRC regulations
You must be a:
- U.S. Citizen,
- U.S. Permanent Resident, or
- Protected individual under 8 U.S.C. 1324b(a)(3) / 22 CFR 120.15
Able to sit and work at a computer for most of the day
Able to lift up to 35 lbs
Willing to travel domestically and internationally as needed
Corrected vision of 20/20

What you’ll get

A senior‑level role with real influence, not just responsibility
The chance to solve meaningful problems and see your work on the production floor
Collaboration with experienced engineers and operations leaders
Competitive compensation and benefits (details shared during the process)

Morgan Advanced Materials is an EEO/AA/M/W/D/V Employer.

Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions of this job.

This job description does not state or imply that all duties to be performed are specifically identified above. Employees are required to follow any other job-related instructions and to perform any other job-related duties requested or instructed by an authorized person of the Company. This document does not create an employment contract, implied or otherwise, other than an “at-will” relationship.

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sr quality engineer jobs in new bedford ma

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