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Quality Engineer Process Engineer Jobs in New York

Quality Engineer

Newark, NJ ยท On-site

$75K - $97K/yr

Quality Engineer Location: New Jersey Duration: Long Term Position Overview We are seeking an ... Support equipment qualification (IQ/OQ/PQ), process validation, cleaning validation, and ongoing ...

Quality Engineer

Fairfield, NJ ยท On-site

$75K - $95K/yr

The Quality Engineer plays a crucial role within a dedicated quality team to ensure manufacturing processes meet rigorous standards through comprehensive quality assurance, audit management, and ...

Process Engineer Join a dynamic team as a Process Engineer, where you will serve as the crucial engineering link between equipment vendors and internal site teams. This role involves supporting ...

Quality Engineer Lead (QEL2)

Clifton, NJ ยท On-site

$95K - $118K/yr

Drive improvements in testing efficiency, automation coverage, engineering processes, and software quality through AI-enabled tooling and continuous improvement initiatives. * Support the development ...

Quality Engineer

Bridgewater, NJ ยท On-site

$73K - $95K/yr

The Quality Engineer serves as a key resource for quality improvement initiatives, statistical ... Evaluate and monitor process capability, inspection methods, control plans, and sampling strategies ...

... engineering and business skills to carry out core functions in a hands-on manufacturing process ... Performs Root Cause/Failure Analysis of products during manufacturing for safety, quality and ...

Quality Engineer

Bridgewater, NJ ยท On-site

$73K - $95K/yr

The Quality Engineer serves as a key resource for quality improvement initiatives, statistical ... Evaluate and monitor process capability, inspection methods, control plans, and sampling strategies ...

Quality Engineer

Bethpage, NY ยท On-site

$70 - $90/hr

Knowledge of inspection requirements associated with processing and finishing (heat treatment ... Quality Engineering scope Includes the development and application of methods and equipment for ...

New

... process development efforts and interaction with part quality. Feedback to corporate engineering ... Adhering to quality system requirements and a focus on continuous improvement * Drive ToolingU ...

Process Development Engineer (Material Science & Formulation) Role Overview We are seeking a ... Collaborate with product development, analytical, and quality teams to ensure all experimental work ...

Quality Engineer Location: Northvale, NJ (On-Site) Pay Rate: $50.00 - $65.00 per hour Employment ... Perform process capability analysis and recommend corrective actions to improve quality and ...

Quality Engineer

Northvale, NJ ยท On-site

$50 - $65/hr

Quality Engineer Location: Northvale, NJ (On-Site) Pay Rate: $50.00 - $65.00 per hour Employment ... Perform process capability analysis and recommend corrective actions to improve quality and ...

Process Engineer

Keyport, NJ ยท On-site

$112K - $143K/yr

Process Development Engineer (Material Science & Formulation) Role Overview We are seeking a ... Collaborate with product development, analytical, and quality teams to ensure all experimental work ...

Quality Engineer

Elmwood Park, NJ ยท On-site

$75K - $97K/yr

The Quality Engineer - Machine Shop is responsible for supporting and improving product quality, process control, inspection readiness, and customer compliance within a precision CNC machining ...

Quality Engineer

Elmwood Park, NJ

$75K - $97K/yr

The Quality Engineer - Machine Shop is responsible for supporting and improving product quality, process control, inspection readiness, and customer compliance within a precision CNC machining ...

New

Quality Engineer

Elmwood Park, NJ

$75K - $97K/yr

The Quality Engineer - Machine Shop is responsible for supporting and improving product quality, process control, inspection readiness, and customer compliance within a precision CNC machining ...

Showing results 21-40

Quality Engineer Process Engineer information

See New York salary details

$37.7K

$94K

$131.8K

How much do quality engineer process engineer jobs pay per year?

As of Aug 20, 2026, the average yearly pay for quality engineer process engineer in New York is $94,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,100.00 and $108,300.00 per year, depending on experience, location, and employer.

What is the difference between Quality Engineer Process Engineer vs Quality Engineer?

AspectQuality EngineerProcess Engineer
Primary FocusQuality assurance, defect prevention, complianceProcess improvement, efficiency, workflow optimization
CertificationsASQ CQE, ISO auditorSix Sigma, Lean certifications
Work EnvironmentManufacturing, production, quality labsManufacturing, engineering, production lines
Common Industry UsageQuality control departmentsProcess improvement teams

While both roles are vital in manufacturing, a Quality Engineer primarily focuses on ensuring product quality and compliance, whereas a Process Engineer concentrates on optimizing manufacturing processes for efficiency. Understanding these differences helps employers and professionals align skills with job requirements effectively.

What cities in New York are hiring for Quality Engineer Process Engineer jobs?

Cities in New York with the most Quality Engineer Process Engineer job openings:

Quality Engineer

Stark Pharma Solutions Inc

Newark, NJ โ€ข On-site

$75K - $97K/yr

Contractor

Re-posted 25 days ago


Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Quality Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Quality Engineer
Location: New Jersey
Duration: Long Term

Position Overview

We are seeking an experienced Quality Engineer to support quality assurance, compliance, validation, and quality systems activities within a pharmaceutical manufacturing environment. This role will focus on ensuring compliance with FDA regulations, cGMP requirements, quality system management, investigations, validation support, and continuous improvement initiatives across manufacturing operations.

Key Responsibilities

• Provide quality oversight for manufacturing operations and ensure compliance with cGMP regulations, FDA requirements, and company quality standards.
• Manage and support quality system activities, including deviations, CAPAs, change controls, non-conformances, and risk assessments.
• Lead and participate in root cause investigations and implement corrective and preventive actions.
• Review and approve manufacturing records, SOPs, validation protocols, reports, and GMP documentation.
• Support equipment qualification (IQ/OQ/PQ), process validation, cleaning validation, and ongoing process verification activities.
• Collaborate with Manufacturing, Engineering, Validation, and Regulatory teams to resolve quality and compliance issues.
• Analyze quality metrics and trends to identify opportunities for process improvements and compliance enhancements.
• Support internal audits, supplier quality programs, customer audits, and regulatory inspections.
• Ensure compliance with 21 CFR Part 210/211, ICH guidelines, GDP, and ALCOA+ data integrity principles.
• Promote a culture of quality through training, compliance awareness, and continuous improvement initiatives.

Required Qualifications

• Bachelor's Degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, Life Sciences, or a related technical discipline.
• 3–5+ years of Quality Engineering, Quality Assurance, Validation, or related experience.
• Experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
• Strong knowledge of quality systems, including deviations, CAPA management, change control, investigations, and risk management.
• Experience supporting equipment qualification, process validation, and manufacturing quality oversight.
• Understanding of cGMP regulations, FDA requirements, data integrity principles, and inspection readiness activities.
• Experience supporting regulatory, customer, or third-party audits is preferred.
• Strong analytical, problem-solving, technical writing, and communication skills.
• Ability to work effectively in a cross-functional team environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/