Top 3 Supplier quality engineer Jobs in Altamont, Ny

Principal Quality engineer
Katalyst Healthcares & Life Sciences —Albany, NY
- Contract
- Hybrid work
- Mentoring
- Senior level
- Leadership
Quick Apply
Principal Engineer, Fuel Cell System Testing
Plug Power Inc. —Slingerlands, NY
- $114,000 - $185,250 a year
- Full-time
- Research
- Office
- Continuous improvement
- Paid holidays
- Dental insurance
Quick Apply
5h
Supplier Quality - Packaging
Wells Enterprises —United States
- $93,959.91 - $131,543.88 a year
- Full-time
- 6 years
- Research
- Bachelor's degree
13d

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Micron —Albany, NY
PhD or MS or equivalent experience with 3+ years of semiconductor industry experience in a related field. The position offers strong technical depth, multi-…
$107,000 - $182,000 a year
Engineering Manager
Minerals Technologies —Adams, MA
Makes final approval of engineering design, cost estimating, and installation of additions, renewals, changes, and improvements to the plant.
$140,000 - $175,000 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
Quick Apply
7d
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
23h

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Principal Quality engineer

Katalyst Healthcares & Life Sciences -
Albany, NY

Quick Apply

Job Details

Contract

Qualifications

Incident investigation techniques for hazard identification
Statistics
Stakeholder engagement
New product introduction engineering projects
Investigations regulatory compliance
Production data analysis
Accreditation standards (regulatory compliance area)
Supplier corrective action implementation
ISO standards
Quality control statistical data analysis
Preventive action implementation
Statistical Process Control
Production deviation management
Corrective and preventive actions (CAPA)
Quality control audit
Vendor compliance audits
Supplier audits
Vendor compliance management
Production validation processes
Quality risk management
Design failure mode and effects analysis (DFMEA)
Supplier development
Regulatory/legal compliance standards in production
Biomedical regulatory compliance
Hazard analysis
Hazard mitigation
Product quality failure
Cross-functional communication
FDA regulations
Audit support

Full Job Description

Job Description:
We are seeking an experienced Principal Quality Engineer to provide technical leadership in quality engineering, regulatory compliance, and continuous improvement initiatives. This role is responsible for driving quality strategy across the product lifecycle, supporting new product development and manufacturing operations, ensuring compliance with applicable regulatory standards, and leading cross-functional quality initiatives. The ideal candidate has extensive experience in regulated industries such as medical devices, pharmaceuticals, or advanced manufacturing and is recognized as a technical expert in Quality Management Systems (QMS), risk management, and process improvement.
Responsibilities:

Provide technical leadership for quality engineering activities across product development, manufacturing, and sustaining engineering.
Lead Quality planning for New Product Introduction (NPI), design transfer, process validation, and manufacturing readiness.
Develop, implement, and continuously improve Quality Management System (QMS) processes in compliance with regulatory and industry standards.
Lead investigations for non-conformances, customer complaints, and quality issues using structured root cause analysis and drive effective CAPA implementation.
Develop and maintain risk management documentation, including Design and Process FMEAs, hazard analysis, and risk mitigation plans.
Support qualification and validation activities, including IQ/OQ/PQ, process validation, and equipment qualification.
Partner with Engineering, Manufacturing, Supply Chain, Regulatory Affairs, and Operations to resolve complex quality issues.
Analyze quality metrics and statistical data to identify trends and implement data-driven process improvements.
Lead supplier quality initiatives, supplier qualification, audits, and corrective action programs.
Ensure compliance with FDA regulations, ISO standards, and applicable global regulatory requirements.
Support internal, customer, and regulatory audits and ensure timely closure of audit observations.
Mentor and coach Quality Engineers while serving as a technical resource for quality-related decisions.
Drive Lean, Six Sigma, and continuous improvement initiatives to improve product quality, reduce defects, and increase operational efficiency.

Requirements:

Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Industrial Engineering, Manufacturing Engineering, Quality Engineering, or a related technical discipline.
10+ years of Quality Engineering experience in a regulated industry such as Medical Devices, Pharmaceuticals, Biotechnology, Aerospace, or Advanced Manufacturing.
Strong knowledge of Quality Management Systems (QMS), quality engineering principles, and regulatory compliance.
Experience with ISO 13485 and/or ISO 9001 Quality Management Systems.
Knowledge of FDA 21 CFR Part 820/QMSR and applicable global quality regulations.
Hands-on experience with CAPA, Non-Conformance (NC), Complaint Handling, Risk Management, FMEA, and Root Cause Analysis.
Experience supporting design transfer, process validation, manufacturing support, and New Product Introduction (NPI).
Proficiency in statistical methods including SPC, MSA, DOE, capability analysis, and data-driven decision making.
Experience leading internal, supplier, customer, and regulatory audits.
Excellent leadership, communication, and stakeholder management skills.

Preferred Qualifications:

ASQ Certified Quality Engineer (CQE), Six Sigma Green Belt or Black Belt certification.
Experience with SAP, Minitab, SmartSolve, TrackWise, or other Quality Management Systems.
Knowledge of Lean Manufacturing, Kaizen, and continuous improvement methodologies.
Experience leading global or cross-functional quality initiatives.
Strong project management and mentoring experience.

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supplier quality engineer jobs in altamont, ny

Principal Quality engineer

Principal Engineer, Fuel Cell System Testing

Supplier Quality - Packaging

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