Quality Engineer Jobs in New Jersey
Quality Engineer jobs in New Jersey are in strong demand across the state's pharmaceutical manufacturing, medical device, aerospace, and consumer electronics sectors, with openings at every level from entry-level quality technician through senior quality engineer and quality manager. The largest concentrations of hiring are in and around Parsippany, Princeton, and Edison, where long-established employers such as Johnson & Johnson, Lockheed Martin, and Becton Dickinson maintain significant operations. The most sought-after specialties in New Jersey include pharmaceutical validation, FDA regulatory compliance, and ISO 9001 quality management systems. Find a role that fits below and apply directly.
Find Quality Engineer JobsOverview
Showing 5 of 78+ Quality Engineer jobs
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.
Intermediate Quality Engineer
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position supports our Princeton, NJ location within the Point of Care business. As an Intermediate Quality Engineer, you’ll partner with Operations to help ensure manufacturing processes, materials, and products meet quality and regulatory requirements. You’ll support validation and qualification activities, investigate quality issues, review production documentation, and assess materials for commercial release while contributing to process improvement and operational excellence.
What You’ll Work On
- Partner with Operations as a Quality representative to review production records, executed test methods, and material disposition decisions before commercial distribution.
- Review process and test method validation, equipment and facility qualification documentation, and calibration records; identify and resolve deficiencies before commercial use.
- Support nonconformance and deviation investigations, assess process risks, recommend mitigations, and help improve manufacturing and quality processes.
- Review and approve standard operating procedures and manufacturing work instructions, and conduct production-area audits to maintain compliance with cGMP, ISO, and internal quality standards.
- Collaborate with cross-functional teams to resolve day-to-day quality concerns, maintain accurate documentation, and support continuous improvement.
Required Qualifications
- Bachelor’s degree in engineering, science or a related field; or an associate degree in a related field with an additional two years of experience
- 2+ years of experience in a manufacturing operations environment
- 1+ years of experience applying quality principles and practices
- Knowledge of and experience working within a 21 CFR Part 820, ISO 13485, and/or cGMP-regulated environment
- Strong communication and collaboration skills with the ability to work effectively across Operations and Quality teams
- Ability to meet applicable PPE requirements and perform role-related physical activities, including lifting up to 40 pounds, with or without reasonable accommodation
- Authorization to work in the United States without sponsorship
Preferred Qualifications
- 2+ years of experience in biotechnology manufacturing, preferably in a GMP and/or ISO 13485 environment
Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.
Intermediate Quality Engineer
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position supports our Princeton, NJ location within the Point of Care business. As an Intermediate Quality Engineer, you’ll partner with Operations to help ensure manufacturing processes, materials, and products meet quality and regulatory requirements. You’ll support validation and qualification activities, investigate quality issues, review production documentation, and assess materials for commercial release while contributing to process improvement and operational excellence.
What You’ll Work On
- Partner with Operations as a Quality representative to review production records, executed test methods, and material disposition decisions before commercial distribution.
- Review process and test method validation, equipment and facility qualification documentation, and calibration records; identify and resolve deficiencies before commercial use.
- Support nonconformance and deviation investigations, assess process risks, recommend mitigations, and help improve manufacturing and quality processes.
- Review and approve standard operating procedures and manufacturing work instructions, and conduct production-area audits to maintain compliance with cGMP, ISO, and internal quality standards.
- Collaborate with cross-functional teams to resolve day-to-day quality concerns, maintain accurate documentation, and support continuous improvement.
Required Qualifications
- Bachelor’s degree in engineering, science or a related field; or an associate degree in a related field with an additional two years of experience
- 2+ years of experience in a manufacturing operations environment
- 1+ years of experience applying quality principles and practices
- Knowledge of and experience working within a 21 CFR Part 820, ISO 13485, and/or cGMP-regulated environment
- Strong communication and collaboration skills with the ability to work effectively across Operations and Quality teams
- Ability to meet applicable PPE requirements and perform role-related physical activities, including lifting up to 40 pounds, with or without reasonable accommodation
- Authorization to work in the United States without sponsorship
Preferred Qualifications
- 2+ years of experience in biotechnology manufacturing, preferably in a GMP and/or ISO 13485 environment
Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
The base pay for this position is $61,300.00 – $122,700.00. In specific locations, the pay range may vary from the range posted.
See All 78 Quality Engineer Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Quality Engineer JobsQuality Engineer Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Quality Engineer Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
- Manufacturing
- Medical Devices
- Energy
What New Jersey Employers Look For
The qualifications that appear most often in quality engineer jobs across New Jersey.
- Bachelor's degree in engineering, manufacturing, or a related technical discipline
- Hands-on experience with quality management systems such as ISO 9001 or AS9100
- Familiarity with FDA 21 CFR regulations and GMP requirements for pharmaceutical or medical device environments
- Proficiency in statistical process control, root cause analysis, and CAPA methodologies
- Experience using inspection tools, measurement equipment, and quality software such as Minitab
- Strong documentation skills and ability to write SOPs, inspection reports, and nonconformance records
Quality Engineer Jobs in New Jersey: Frequently Asked Questions
How do you become a quality engineer in New Jersey?
Most quality engineer roles in New Jersey require a bachelor's degree in mechanical, industrial, electrical, or manufacturing engineering, though some employers accept a closely related technical field. New Jersey does not require a state-issued license specifically for quality engineers, but professional certifications such as the ASQ Certified Quality Engineer credential are widely expected and carry real weight with New Jersey's pharmaceutical, aerospace, and medical device employers. Strong candidates also build familiarity with FDA regulatory frameworks before applying.
Which companies hire quality engineers in New Jersey?
Employers hiring quality engineers in New Jersey right now include CooperSurgical, Katalyst Healthcares & Life Sciences, and Lockheed Martin, based on current listings on Migrate Mate as of November 2026. New Jersey's dense concentration of pharmaceutical headquarters and contract manufacturing organizations means quality engineering talent is consistently in demand across both large corporations and mid-size suppliers operating under FDA oversight.
Which New Jersey cities have the most quality engineer jobs?
The cities with the most quality engineer openings in New Jersey are Livingston, Moorestown, and Camden. This distribution reflects where New Jersey's largest pharmaceutical campuses, aerospace facilities, and medical device manufacturers are anchored, with suburban corridors like the Route 1 technology corridor near Princeton and the Morris County life sciences cluster driving a significant share of listings outside the major urban centers.
Are there remote quality engineer jobs in New Jersey?
Yes, but they're rare. Quality engineering work is largely hands-on, involving production floor inspections, equipment calibration, and in-person audits that cannot be performed remotely. About 40% of quality engineer openings tied to New Jersey are remote or hybrid as of November 2026. The portions of the role most likely to allow remote work include documentation review, supplier quality audits conducted by video, and regulatory compliance writing.
How can I get hired as a quality engineer in New Jersey with little or no experience?
The most realistic entry path is through a quality technician or quality inspector role at one of New Jersey's many pharmaceutical contract manufacturers or consumer goods facilities, where hands-on inspection experience is valued over advanced credentials. Employers such as major Parsippany-area pharma companies and Edison-based manufacturers regularly hire associate quality engineers from adjacent positions in production, laboratory operations, or supply chain. Earning an ASQ Certified Quality Technician credential before applying adds a concrete advantage and demonstrates seriousness to hiring managers.
Where can I find and apply to quality engineer jobs in New Jersey?
You can find and apply to quality engineer jobs in New Jersey on Migrate Mate, which lists current openings from employers hiring across the state. Search the listings to find roles that match your experience level, specialization, and preferred location, then apply directly to the ones that fit.
See All 78 Quality Engineer Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Quality Engineer Jobs