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Quality Assurance Associate Jobs in Riverside, NJ

Jj

QA Associate II

Malvern, PA

Malvern, Pennsylvania, United States of America, Spring House, Pennsylvania, United States of America Johnson and Johnson Innovative Medicine, is recruiting for a QA Associate II! This position will ...

New

Jj

QA Associate II

Spring House, PA · On-site

Malvern, Pennsylvania, United States of America, Spring House, Pennsylvania, United States of America Johnson and Johnson Innovative Medicine, is recruiting for a QA Associate II! This position will ...

New

Abzena Inc.

Sr QA Associate, Operations

Bristol, PA · On-site

The Senior Associate, QA Operations is responsible for providing quality oversight of GMP manufacturing and development activities through direct quality presence on the manufacturing floor and ...

Abzena Inc.

QA Associate II, Operations

Bristol, PA · On-site

The Associate II, Quality Operations provides day-to-day QA oversight and documentation review to support GMP manufacturing of intermediates and drug substances. The role ensures production ...

Veranova L P

Senior QA Associate

Paulsboro, NJ · On-site

$90K - $115K/yr

A minimum of 5 years in QA/QC/Compliance in an FDA/DEA regulated environment or a minimum of 5-7 years in API manufacturing in an FDA/DEA regulated environment is desired. * The ability to exercise ...

Abzena Inc.

QA Associate I/II, Compliance

Bristol, PA · On-site

The Associate (I/II), QA Compliance is responsible for supporting site compliance and ensuring that GMP document control is maintained in a state of control in accordance with Quality policies and ...

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All JobsQuality Assurance Associate JobsQuality Assurance Associate Jobs in Riverside, NJ

Quality Assurance Associate information

See Riverside, NJ salary details

$13

$29

$62

How much do quality assurance associate jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for quality assurance associate in Riverside, NJ is $29.58, according to ZipRecruiter salary data. Most workers in this role earn between $18.94 and $34.71 per hour, depending on experience, location, and employer.

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.

Which pays more, QA or QC?

In the quality assurance (QA) and quality control (QC) fields, QA roles typically offer higher salaries because they involve broader responsibilities such as process improvement and compliance management. QC positions often focus on inspecting and testing products, which may have lower pay scales. Salary differences can vary based on industry, experience, and certifications like Six Sigma or ISO standards.

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 some 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 qualifications do you need to be a QA?

To become a Quality Assurance Associate, candidates typically need a high school diploma or equivalent, with many roles preferring a bachelor's degree in a related field such as quality assurance, engineering, or computer science. Strong attention to detail, analytical skills, and familiarity with testing tools or software are important, along with good communication skills. Certifications like ISTQB can enhance prospects but are not always required.

Is QA a good entry level job?

Quality Assurance Associate roles are often suitable for entry-level candidates, as they typically require attention to detail, basic understanding of testing processes, and familiarity with tools like test management software. These positions can provide valuable industry experience and opportunities for skill development in areas such as software testing, documentation, and quality standards.

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

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 the most commonly searched types of Quality Assurance jobs in Riverside, NJ? The most popular types of Quality Assurance jobs in Riverside, NJ are:
What cities near Riverside, NJ are hiring for Quality Assurance Associate jobs? Cities near Riverside, NJ with the most Quality Assurance Associate job openings:
Quality Assurance Associate jobs near you
Infographic showing various Quality Assurance Associate job openings in Riverside, NJ as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $61,533 per year, or $29.6 per hour.

QA Associate II

Jj

Malvern, PA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Quality Assurance

Job Category:

Professional

All Job Posting Locations:

Malvern, Pennsylvania, United States of America, Spring House, Pennsylvania, United States of America

Job Description:

Johnson and Johnson Innovative Medicine, is recruiting for a QA Associate II! This position will be located in Malvern, PA with considerations given to Spring House, PA.

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

On this team, we provide end to end quality oversight of GMP manufacturing areas. You will act as a liaison with other internal quality organizations to standardize policies, practices and procedures to increase quality and compliance and champion increased awareness of quality related concerns.

Main responsibilities will include, but are not limited to:
  • Partner with Research & Development and Supply Chain teams to support GMP manufacture of clinical products, medias, and buffers.
  • Collaborate with business partners to support new product introductions .
  • Perform regularly scheduled oversight of manufacturing areas and on-call support as assigned.
  • Review and approve controlled documents including standard operating procedures, work instructions, and risk assessments.
  • Ensure all non-conformances are fully investigated and effective corrective/preventive actions are implemented in a timely manner.
  • Support change management processes including formal change controls by evaluating the proposed changes, assessing impact, and providing quality input on implementation plans.
  • Perform batch record review and critical alarm review.
  • Support in process improvement activities including assessing current processes, providing improvement input and working with partners to implement changes.
  • Support site inspections and inspection readiness activities.
  • Other duties may be assigned as necessary.
Qualifications

Education:

A minimum of a Bachelor's Degree is required with a focus in Engineering, Biology, Biochemistry, Microbiology, Chemistry, or relevant scientific field/equivalent technical field preferred.

Required:

  • At least 3 years of experience in a regulated manufacturing environment, preferably in biotechnology or pharmaceutical industry.
  • Ability to maintain written records of work performed in paper-based and computerized quality systems.
  • Ability to work independently on routine tasks and require some supervision on complex issues.
  • Ability to be organized and capable of working in a team environment with a positive demeanor.
  • A high degree of accuracy and attention to detail, and excellent interpersonal, oral and written communication skills.
  • Working knowledge of cGMP regulations and FDA/EU guidance related to biologics and cell banking
Preferred
  • Experience in Quality or Manufacturing for Large Molecule Manufacturing
  • Working knowledge of Phase Appropriate GMP practices.
  • Experience with document reviews and regulatory inspection processes is preferred.
  • Ability to prioritize daily business needs while being flexible and adaptable to frequently shifting priorities.
Other:
  • This position is located primarily in Malvern, PA, but may require up to 20% domestic travel to the Johnson and Johnson Innovative Medicine site in Spring House, PA.
  • Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
  • Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
  • This position is eligible to participate in the Company's long-term incentive program.
  • Employees are eligible for the following time off benefits:
  • Vacation - up to 120 hours per calendar year
  • Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
  • Holiday pay, including Floating Holidays - up to 13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

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