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Quality Assurance Qa Associate Jobs (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 ...

The Quality Assurance Associate performs activities associated with quality control of meals. You will be responsible for ensuring the safety of our meals in accordance with our HACCP and FDA ...

... QA support Qualifications: BA/BS in Biology, Chemistry, Microbiology, Engineering, or a related field is required (no prior work experience needed). Alternatively, an Associate's degree with up to 2 ...

Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great ...

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 ...

Basic Function Based out of Industrial Oils Unlimited, LLC , located in Tulsa, Oklahoma and reporting to the Director of Manufacturing Operations, the Quality Assurance Associate examines products ...

New

Basic Function Based out of Industrial Oils Unlimited, LLC , located in Tulsa, Oklahoma and reporting to the Director of Manufacturing Operations, the Quality Assurance Associate examines products ...

New

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Quality Assurance Qa Associate information

See salary details

$12

$29

$62

How much do quality assurance qa associate jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for quality assurance qa associate in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What does a Quality Assurance (QA) Associate do?

A Quality Assurance (QA) Associate is responsible for ensuring that products or services meet established quality standards and regulatory requirements. They develop and implement testing procedures, conduct inspections, and identify areas for improvement in production or service processes. QA Associates work closely with other departments to resolve quality-related issues and help maintain compliance with company policies and industry regulations. Their work is essential for delivering consistent, safe, and effective products to customers.

How does a Quality Assurance QA Associate typically interact with other departments to ensure product quality?

Quality Assurance QA Associates frequently collaborate with teams such as Production, Research & Development, and Regulatory Affairs to uphold product quality standards. They review documentation, provide feedback on process improvements, and may participate in cross-functional meetings to address quality concerns or deviations. This teamwork is essential for identifying potential issues early, ensuring compliance with regulations, and supporting a culture of continuous improvement throughout the organization.

What are the key skills and qualifications needed to thrive as a Quality Assurance (QA) Associate, and why are they important?

To thrive as a Quality Assurance QA Associate, you need a strong understanding of quality control processes, documentation standards, and often a degree in a scientific or technical field. Familiarity with quality management systems (such as ISO standards), proficiency in data analysis tools, and experience with software like LIMS or ERP systems are typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for this position. These skills ensure products meet regulatory requirements and company standards, ultimately protecting consumer safety and business reputation.

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

AspectQuality Assurance Qa AssociateQuality Control Inspector
Primary FocusPreventing defects through process improvementsDetecting defects in finished products
Work EnvironmentCollaborates with teams, audits, documentationInspects products on production lines or in labs
CertificationsOften requires QA certifications, ISO standards knowledgeMay require specific industry certifications, safety training
Industry UsageCommon in manufacturing, software, healthcarePrimarily in manufacturing, food, electronics

The main difference is that a Quality Assurance Qa Associate focuses on preventing defects through process improvements and audits, while a Quality Control Inspector primarily detects defects in finished products. QA associates work proactively to ensure quality standards are met, whereas QC inspectors verify product quality after production. Both roles are essential in maintaining product standards but serve different points in the quality management process.

More about Quality Assurance Qa Associate jobs
What cities are hiring for Quality Assurance Qa Associate jobs? Cities with the most Quality Assurance Qa Associate job openings:
What are the most commonly searched types of Quality Assurance Qa jobs? The most popular types of Quality Assurance Qa jobs are:
What states have the most Quality Assurance Qa Associate jobs? States with the most job openings for Quality Assurance Qa Associate jobs include:
Infographic showing various Quality Assurance Qa Associate job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 98% Full Time, and 1% Part Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

QA Associate

Novartis

Morris Plains, NJ • On-site

$62K - $94K/yr

Full-time

Medical, Retirement, PTO

Posted 9 days ago


Novartis rating

7.4

Company rating: 7.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

53rd of 71 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