Top 6 Supplier quality engineer Jobs in White River Junction Vt

Quality Engineer
Nolato —South Royalton, VT
- $75,000 - $110,000 a year
- Full-time
- Engineering
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Quality Engineer - Manufacturing
Jabil Circuit —Claremont, NH
- Full-time
- Mid-level
- Bachelor's degree
- Training & development
- Commuter assistance
- Health savings account
Quality Engineer - LED Lighting Products
LEDdynamics —Randolph, VT
- Full-time
- Engineering
- Mid-level
- Office
Quick Apply
Staff Quality Engineer
Hypertherm —Lebanon, NH
- $93,936 - $156,562 a year
- Full-time
- Bachelor of Science
- Travel
- Mentoring
- Profit sharing
- Employee stock ownership plan
Quality Engineer Trainer
Insituform Technologies, LLC —Bethel, VT
- From $75,000 a year
- Full-time
- Microsoft Excel
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
Supplier Quality - Packaging
Wells Enterprises —United States
- $93,959.91 - $131,543.88 a year
- Full-time
- 6 years
- Research
- Bachelor's degree
14d

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Quality Manager
Leddy Group —Tilton, NH
Ensure raw materials, components, in-process and finished products meet customer specifications and established quality standards.
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Quality Manager
Edare —Lebanon, NH
Certified Quality Auditor (CQA) certification or ability and desire to obtain CQA certification. While our immediate need revolves around standing up an AS 9100…
$115,000 - $140,000 a year
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Supplier Quality Engineer
Nifco America, Corp. —Canal Winchester, OH
ASQ or equivalent certification or training (CQE, LSS Belt, etc). IATF certification for Internal or Lead auditor with documentation available.
$70,000 - $88,000 a year
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8d
Supplier Quality Engineer
Honda —Raymond, OH
Provide technical assessment and support throughout tool trials and crisis activity, as needed. Prepare, develop, and manage approval of part conformance prior…
$71,100 - $106,600 a year
2d

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supplier quality engineer jobs near white river junction vt

Quality Engineer

Nolato -
South Royalton, VT

Quick Apply

Job Details

Full-time
$75,000 - $110,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Parental leave
Employee assistance program
Vision insurance
401(k) matching
Life insurance
Referral program

Qualifications

GD&T
Bachelor's degree
Medical device manufacturing facility experience
SolidWorks
Quality engineering
Regulatory/legal compliance standards in production
Biomedical regulatory compliance
Quality improvement programs in engineering
Continuous process improvement (CPI)
ISO 13485

Full Job Description

Serve as a high-velocity technical lead within the Vermont Operations quality engineering pool. This role is responsible for the full lifecycle of quality engineering across both facilities, ensuring 100% adherence to ISO 13485 and FDA 21 CFR 820 requirements. This position is a resource, capable of deployment in any facility to lead validations, investigations, and process Controls.

Core Responsibilities

-Advanced Investigations (NC/CAPA): Lead complex nonconformance investigations using standardized Root Cause Analysis (RCA) tools (5-Why, Fishbone) to identify systemic breakdowns and ensure effective corrective actions.

-Process & Product Validations: Develop, execute, and write protocols and reports for IQ/OQ/PQ validations, including injection molding, secondary operations, and auxiliary manufacturing processes.

-Statistical Intervention (SPC): Beyond just "monitoring" data, the QE is responsible for establishing Statistical Process Control (SPC) alert thresholds and leading the technical intervention before a process drifts into a nonconformance.

-Software Validation (CSV): Coordinate and oversee Software Validation (CSV) for eQMS, MQ1, and production-related software to ensure data integrity and regulatory compliance.

-Supplier Development & Control: Manage the Approved Supplier List (ASL), execute critical supplier audits, and lead the Supplier Corrective Action Request (SCAR) process.

-Statistical Control: Implement and maintain Statistical Process Control (SPC), Gage R&R (MSA) studies, and process capability studies to ensure measurement system reliability.

-Design for Manufacturability (DFM) Support: The QE must participate in product design reviews to provide the "Quality Voice," ensuring that new products are actually capable of being inspected and validated with the existing technical pool's resources.

Technical QC Oversight: Provide structural and technical oversight to the Quality Control (QC) vertical, resolving floor quality issues and improving inspection gauging efficiencies.

-Regulatory Submission Support: Manage technical file inputs, regulatory requests, and technical file integrity to support global market readiness.

-Tooling & Equipment Handover: The QE must act as the "Gatekeeper" for Tooling Acceptance, ensuring that any new or repaired mold or auxiliary equipment has a completed and verified validation package before being released to the production floor.

-Training & Competency: Perform technical training for Quality Assurance Technicians (QATs) and serve as a Subject Matter Expert (SME) for hands-on competency assessments.

Qualifications & Skills

-Education & Experience: * Bachelor’s degree in Engineering or Science OR 4–7 years of direct experience in the Quality Engineering medical device field.

-Experience: Minimum 4–7 years of experience specifically within a medical device or highly regulated FDA environment.

-Knowledge: Expert understanding of FDA 21 CFR 820, ISO 13485, GD&T, and MSA.

-Tools: Proficiency in Minitab, Solidworks, MS suite, ERP and eQMS systems.

-Requirements: Ability to lift up to 60 lbs and travel between local facilities for technical deployment.

-Excellent communication, time management and organizational skills.

-Ability to manage multiple priorities.

-Must be able to function well in a team-oriented environment.

-Flexibility to work additional hours when needed.

-Professional appearance.

-Must have a continuous improvement mindset.

Job Type: Full-time

Pay: $75,000.00 - $110,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Life insurance
Paid time off
Parental leave
Referral program
Tuition reimbursement
Vision insurance

People with a criminal record are encouraged to apply

Experience:

medical device or highly regulated FDA environment: 4 years (Required)
expert knowledge of FDA 21 CFR 820, ISO 13485, GD&T, MSA: 4 years (Required)

Ability to Relocate:

South Royalton, VT 05068: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Refine Your Search

supplier quality engineer jobs in white river junction vt

Quality Engineer

Quality Engineer - Manufacturing

Quality Engineer - LED Lighting Products

Staff Quality Engineer

Quality Engineer Trainer

Supplier Quality - Packaging

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