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Quality Assurance Associate Jobs in Edison, NJ (NOW HIRING)

QA Associate

Morris Plains, NJ · On-site

$62K - $94K/yr

The QA Associate will interact directly with site staff, who are performing the daily operational functions in support of their effort to produce quality products. This role ensures that the quality ...

QA Associate

Morris Plains, NJ · On-site

$62K - $94K/yr

The QA Associate will interact directly with site staff, who are performing the daily operational functions in support of their effort to produce quality products. This role ensures that the quality ...

QA Associate

East Windsor, NJ · On-site

$52K - $70K/yr

... Quality Assurance Minimum Field of Expertise • Computer skills • Previous work in a regulated environment • Problem solving skills • Ability to coordinate multiple tasks in a fast-paced ...

QA Associate

East Windsor, NJ · On-site

$52K - $70K/yr

... in Quality Assurance Minimum Field of Expertise Computer skills Previous work in a regulated environment Problem solving skills Ability to coordinate multiple tasks in a fast-paced environment ...

Overview The Quality Assurance Associate is responsible for assisting the QA team with day-to-day functions related to the first run of production, dual / second sourcing review and auditing current ...

QA Team Lead

East Windsor, NJ · On-site

$80K - $100K/yr

In addition to individual contributor responsibilities, this role provides day-to-day leadership to QA Associates, including work planning, performance management, and oversight of team deliverables ...

QA Team Lead

East Windsor, NJ · On-site

$80K - $100K/yr

In addition to individual contributor responsibilities, this role provides day-to-day leadership to QA Associates, including work planning, performance management, and oversight of team deliverables ...

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Quality Assurance Associate information

See Edison, NJ salary details

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How much do quality assurance associate jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for quality assurance associate in Edison, NJ is $30.32, according to ZipRecruiter salary data. Most workers in this role earn between $19.42 and $35.58 per hour, depending on experience, location, and employer.

What does a quality assurance associate do?

A Quality Assurance Associate is responsible for monitoring and evaluating the various processes involved in product development and production to ensure they meet established quality standards. Their duties typically include conducting inspections, documenting findings, assisting in process improvements, and ensuring compliance with regulatory requirements. They play a critical role in identifying defects, reducing errors, and maintaining the overall quality of products or services before they reach customers.

What skills and qualifications are needed to be a quality assurance associate?

To excel as a Quality Assurance Associate, you need a solid understanding of quality control principles, attention to detail, and often a degree in a related field like chemistry, biology, or engineering. Familiarity with industry-standard quality management systems (such as ISO 9001), statistical analysis software, and documentation tools is typically required. Strong problem-solving skills, effective communication, and the ability to work collaboratively are highly valued in this role. These skills ensure that products and processes consistently meet standards, reduce errors, and maintain compliance with regulatory requirements.

What are common challenges faced by quality assurance associates in ensuring consistent product quality?

Quality Assurance Associates often encounter challenges such as managing tight production deadlines while maintaining thorough testing standards, addressing unexpected defects, and adapting quickly to new regulatory or product requirements. Effective communication with production, development, and regulatory teams is crucial for resolving issues efficiently. Staying current with evolving quality standards and continuously improving testing processes are also important for success in this role.

What is the difference between Quality Assurance Associate vs Quality Control Inspector?

AspectQuality Assurance AssociateQuality Control Inspector
CertificationsOften requires certifications like ASQ CQIA or related quality assurance trainingMay require certifications such as ISO auditor or specific industry standards
Work EnvironmentInvolves process audits, documentation, and improving quality systemsFocuses on inspecting products or materials for defects
Employer & Industry UsageCommon in manufacturing, pharmaceuticals, and tech industriesPrimarily in manufacturing, food production, and assembly lines

While both roles focus on quality, the Quality Assurance Associate emphasizes developing and maintaining quality systems and processes, whereas the Quality Control Inspector concentrates on inspecting products for defects. Both roles are essential for ensuring product quality but differ in scope and responsibilities.

Is a Quality Assurance Associate an entry-level job?

A Quality Assurance Associate position is often considered entry-level, suitable for candidates with little to no prior experience in quality assurance or related fields. It typically requires basic knowledge of testing procedures, attention to detail, and may involve training on specific tools or software used in quality control processes.

What is the role of a quality assurance associate?

A quality assurance associate is responsible for monitoring and testing products or services to ensure they meet quality standards and specifications. They often develop testing procedures, document issues, and collaborate with teams to improve processes, using tools like checklists and quality management systems. Attention to detail and knowledge of industry regulations are essential for this role.

What are the most commonly searched types of Quality Assurance jobs in Edison, NJ?

The most popular types of Quality Assurance jobs in Edison, NJ are:

What are popular job titles related to Quality Assurance Associate jobs in Edison, NJ?

For Quality Assurance Associate jobs in Edison, NJ, the most frequently searched job titles are:

What cities near Edison, NJ are hiring for Quality Assurance Associate jobs?

Cities near Edison, NJ with the most Quality Assurance Associate job openings:

Infographic showing various Quality Assurance Associate job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $63,072 per year, or $30.3 per hour.

QA Associate

Novartis

Morris Plains, NJ • On-site

$62K - $94K/yr

Full-time

Medical, Retirement, PTO

Re-posted yesterday


Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

Job Description Summary

Job Description Summary
The Quality Operations Associate is responsible for first level, hands on, day-to-day cGMP facilitator role for all site related GMP activities. The QA Associate will interact directly with site staff, who are performing the daily operational functions in support of their effort to produce quality products. This role ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality.


Job Description

Hours & Shifts Available:

Sun-Wed 6:00am-4:30pm

Sun-Wed 12:00pm-10:00pm

Wed-Sat 6:00am-4:30pm

Wed-Sat 12:00pm-10:00pm

Number of positions available: 7

Location: This role is on-site and located in Morris Plains, NJ

Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you.

Major accountabilities:

Under the guidance of the Quality Assurance Manager provides oversight to various departments within Morris Plains.

  • Review and approve batch records, Apheresis, Aborted and Invalid Assays, etc. to ensure adherence to Novartis policies, SOPs, and cGMP requirements.

  • Conduct routine shop floor tasks related to aseptic operations including but not limited to ViMOS, APV program observations, walkthrough program, QA area release, etc.

  • Under the guidance of the Quality Assurance Managers, perform triaging and initiatition of events (Quality Event, Deviation, Action, CAPA, etc.). Expected to work with and partner with cross functional departments during triaging.

  • Actively engage in process improvement and Right First-Time initiatives at the Morris Plains site. Ensures adherence of appropriate regulations and Novartis quality standards.

  • Write and/or review of Standard Operating Procedures (SOPs), as needed.

  • Assist in providing documentation as needed for self-inspections and external audits.

  • Champion a Quality Culture and ensure a safe working environment.

  • Complete job-related training as required.

  • Demonstrates and role models the Novartis values and behaviors.

Minimum Requirements:

Education:

  • BA degree in Biological Sciences; or Associates Degree; or equivalent relevant career experience may be accepted with a minimum of 2 years of experience in a pharmaceuticals environment.
  • Knowledge and understanding of cGMPs, keeping up to date with current industry issues and changing regulations.
  • Excellent oral and written communication skills required.
  • Demonstrate ownership of completing daily tasks and excellent interpersonal skills.
  • Ability to work under direction of team members, independently, and as part of a team if necessary.
  • SAP, 1QEM, MES, LIMS knowledge preferred

Languages:

  • English

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

The pay range for this position at commencement of employment is expected to be between $62,900 and $94,300/year; however, while salary ranges are effective from 1/1/24 through 12/31/24, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

Handbook. https://www.novartis.com/careers/benefits-rewards


Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patient and communities we serve.

Join our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:
https://talentnetwork.novartis.com/network


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$55,000.00 - $102,200.00


Skills Desired

Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

What Novartis employees say

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Benefits

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