Quality Specialist Jobs in New Jersey
Quality Specialist jobs in New Jersey are concentrated in pharmaceuticals, medical devices, and food manufacturing, three sectors where New Jersey commands national significance and where demand for quality professionals remains consistently strong from entry-level inspector through senior quality engineer. The heaviest hiring is in and around Newark, Princeton, and the Route 1 corridor, where major employers such as Johnson & Johnson, Merck, and Becton Dickinson maintain long-established operations. Regulatory compliance, supplier quality management, and validation engineering are the most in-demand specialties across these industries. See the openings below and apply to the ones that match your experience.
Find Quality Specialist JobsOverview
Showing 5 of 45+ Quality Specialist jobs
Position Summary
The Quality Specialist is responsible for compiling, reviewing, and maintaining quality documentation and customer data packages to ensure compliance with customer and regulatory requirements. Working closely with Quality, Manufacturing, Planning, Shipping, and Customer Service teams, this role supports documentation accuracy, product quality, and on-time customer deliveries.
Responsibilities
- Compiles data packages and certificates per customer requirements, including initiating the package at top-level kit release and organizing all documentation for final shipment.
- Review data packages for completeness, legibility, revision-level accuracy, and configuration compliance before customer submission.
- Responsible for coordinating & witnessing customer/DCMA visits per quality plans and purchase order requirements.
- Sign off on the job traveler, data package, and Certificate of Conformance (CofC) once all items are verified as complete.
- Work with customer service, shipping, and planning on RMA. Receive parts in by reviewing warranty status and documenting as-is part condition
- Communicate and escalate with the internal team about general quality issues and issue nonconformance products.
- Assist Quality Engineers and Quality Managers where needed.
Job Requirements
- High school diploma or equivalent; Associate degree preferred
- 2+ years in aerospace/defense manufacturing documentation or quality assurance
- Demonstrated experience compiling controlled documentation packages (travelers, CoFCs, test records, material certs)
- Able to read specifications, drawings, prints, and schematics.
- Experience with customer websites and portal is a plus.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook). and Adobe (pdf merging and moving documents digitally)
- Must be detail oriented and have good communication and organizational skills.
Preferred Skills
- Knowledge of aerospace quality standards and manufacturing processes.
- Experience supporting customer and government audits.
- Familiarity with document control and configuration management practices.
- Ability to work independently and collaboratively across departments.
- Strong record-keeping and compliance management skills.
Physical Requirements
- Ability to sit, stand, and work at a computer for extended periods.
- Ability to occasionally lift and move documentation boxes or materials up to 25 pounds.
- Ability to work in both office and manufacturing environments as needed.
Valcor's strength and reputation are the result of delivering cutting-edge, reliable products to customers with unique and hard-to-handle applications. Our heritage of more than seven decades of technical innovation and reliable performance is brought to bear on each and every product. Valcor's staff takes pride in applying their skills, with the latest technology and equipment, to create truly superior offerings.
Valcor is much more than just a place to work. Valcor has cultivated a unique environment – called “One Valcor” where employees are both technically challenged and experience the everyday benefits of a successful company in the aircraft, space, and industrial segments. We work hard as the “One Valcor” team and it is demonstrated by our more 60 years of continued success.
Come join our team and experience the rewards of our experience and innovation
All candidates must meet the US persons criteria.
Please note: The salary range is based on our market pay structure. However, individual salaries are determined by a variety of factors including, but not limited to, business considerations, local market conditions, and internal equity, as well as candidate qualifications, such as skills, education, and experience.
Employee Benefits: At Valcor Engineering, we support our employees in all aspects of their life, including their health and financial well-being. Regular employees scheduled to work 30+ hours per week are offered: health, dental, and vision insurance; health savings accounts; a 401(k) savings plan; long term disability coverage; and life and accident insurance. We also have an employee assistance program. Our leave programs include Vacation and PTO time off, paid holidays, as well as other types such as bereavement, and any applicable federal and state sick leave. Employees may participate in the company recognition program to receive monetary or non-monetary recognition awards.
We are an equal opportunity employer and do not discriminate on the basis of race, color, religion, sex, national origin, age, disability, genetic information, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. All qualified applicants will be considered for employment without regard to these characteristics.
Position Summary
The Quality Specialist is responsible for compiling, reviewing, and maintaining quality documentation and customer data packages to ensure compliance with customer and regulatory requirements. Working closely with Quality, Manufacturing, Planning, Shipping, and Customer Service teams, this role supports documentation accuracy, product quality, and on-time customer deliveries.
Responsibilities
- Compiles data packages and certificates per customer requirements, including initiating the package at top-level kit release and organizing all documentation for final shipment.
- Review data packages for completeness, legibility, revision-level accuracy, and configuration compliance before customer submission.
- Responsible for coordinating & witnessing customer/DCMA visits per quality plans and purchase order requirements.
- Sign off on the job traveler, data package, and Certificate of Conformance (CofC) once all items are verified as complete.
- Work with customer service, shipping, and planning on RMA. Receive parts in by reviewing warranty status and documenting as-is part condition
- Communicate and escalate with the internal team about general quality issues and issue nonconformance products.
- Assist Quality Engineers and Quality Managers where needed.
Job Requirements
- High school diploma or equivalent; Associate degree preferred
- 2+ years in aerospace/defense manufacturing documentation or quality assurance
- Demonstrated experience compiling controlled documentation packages (travelers, CoFCs, test records, material certs)
- Able to read specifications, drawings, prints, and schematics.
- Experience with customer websites and portal is a plus.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook). and Adobe (pdf merging and moving documents digitally)
- Must be detail oriented and have good communication and organizational skills.
Preferred Skills
- Knowledge of aerospace quality standards and manufacturing processes.
- Experience supporting customer and government audits.
- Familiarity with document control and configuration management practices.
- Ability to work independently and collaboratively across departments.
- Strong record-keeping and compliance management skills.
Physical Requirements
- Ability to sit, stand, and work at a computer for extended periods.
- Ability to occasionally lift and move documentation boxes or materials up to 25 pounds.
- Ability to work in both office and manufacturing environments as needed.
Valcor's strength and reputation are the result of delivering cutting-edge, reliable products to customers with unique and hard-to-handle applications. Our heritage of more than seven decades of technical innovation and reliable performance is brought to bear on each and every product. Valcor's staff takes pride in applying their skills, with the latest technology and equipment, to create truly superior offerings.
Valcor is much more than just a place to work. Valcor has cultivated a unique environment – called “One Valcor” where employees are both technically challenged and experience the everyday benefits of a successful company in the aircraft, space, and industrial segments. We work hard as the “One Valcor” team and it is demonstrated by our more 60 years of continued success.
Come join our team and experience the rewards of our experience and innovation
All candidates must meet the US persons criteria.
Please note: The salary range is based on our market pay structure. However, individual salaries are determined by a variety of factors including, but not limited to, business considerations, local market conditions, and internal equity, as well as candidate qualifications, such as skills, education, and experience.
Employee Benefits: At Valcor Engineering, we support our employees in all aspects of their life, including their health and financial well-being. Regular employees scheduled to work 30+ hours per week are offered: health, dental, and vision insurance; health savings accounts; a 401(k) savings plan; long term disability coverage; and life and accident insurance. We also have an employee assistance program. Our leave programs include Vacation and PTO time off, paid holidays, as well as other types such as bereavement, and any applicable federal and state sick leave. Employees may participate in the company recognition program to receive monetary or non-monetary recognition awards.
We are an equal opportunity employer and do not discriminate on the basis of race, color, religion, sex, national origin, age, disability, genetic information, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. All qualified applicants will be considered for employment without regard to these characteristics.
See All 45 Quality Specialist Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Quality Specialist JobsQuality Specialist Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Quality Specialist 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
- Medical Devices
- Science & Research
- Construction & Real Estate
What New Jersey Employers Look For
The qualifications that appear most often in quality specialist jobs across New Jersey.
- Bachelor's degree in engineering, life sciences, or a related technical field required
- Working knowledge of FDA regulations and Good Manufacturing Practices (GMP) preferred
- Experience with quality management systems such as ISO 9001 or ISO 13485
- Proficiency conducting internal audits, root cause analysis, and CAPA procedures
- Familiarity with statistical process control tools and quality inspection methods
- Strong written communication skills for preparing deviation reports and SOPs
Quality Specialist Jobs in New Jersey: Frequently Asked Questions
How do you become a quality specialist in New Jersey?
Most quality specialist roles in New Jersey require a bachelor's degree in engineering, life sciences, chemistry, or a related field, particularly given the dominance of pharmaceutical and medical device employers in the state. There is no single state-issued license for the role, but industry certifications from the American Society for Quality, such as the Certified Quality Auditor or Certified Quality Engineer, are widely recognized by New Jersey employers and can significantly strengthen a candidacy in regulated industries.
Which companies hire quality specialists in New Jersey?
Employers hiring quality specialists in New Jersey right now include Hackensack Meridian Health, SGS, and LTM Limited, based on current listings on Migrate Mate as of August 2026. New Jersey's dense concentration of pharmaceutical, biotech, and medical device manufacturers means quality roles appear regularly at both large multinational corporations and specialized contract manufacturing organizations throughout the state.
Which New Jersey cities have the most quality specialist jobs?
Bridgewater, Piscataway, and Edison account for the largest share of quality specialist openings in New Jersey. The concentration reflects the Route 1 pharmaceutical corridor anchoring the Princeton and New Brunswick area, Newark's proximity to major logistics and manufacturing hubs, and the sustained presence of life sciences and medical device employers that have operated campuses in central and northern New Jersey for decades.
Are there remote quality specialist jobs in New Jersey?
Yes, but they're rare. Quality specialist work is largely hands-on, requiring on-site inspections, equipment validation, and direct involvement in production environments, which limits remote options significantly. About 40% of quality specialist openings tied to New Jersey are remote or hybrid as of August 2026, and those positions tend to involve supplier quality management, documentation review, or audit coordination rather than floor-level quality control.
How can I get hired as a quality specialist in New Jersey with little or no experience?
The most realistic entry path is a quality technician or quality inspector role at one of New Jersey's many contract manufacturing or pharmaceutical packaging facilities, where employers regularly hire candidates with a relevant associate or bachelor's degree and train on internal systems. Large employers such as Johnson & Johnson and Merck run co-op and rotational programs that bring in candidates without direct quality experience. Earning an entry-level American Society for Quality certification before applying gives candidates a measurable edge over others at the same experience level.
Where can I find and apply to quality specialist jobs in New Jersey?
You can find and apply to quality specialist jobs in New Jersey on Migrate Mate, which lists current openings from employers actively hiring in the state. Search the listings to find roles that match your background and experience level, then apply directly to the ones that fit.
See All 45 Quality Specialist Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Quality Specialist Jobs