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Quality Control Associate Jobs in New Jersey (NOW HIRING)

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Maintain required training and training records and provide training to qualify other associates ... Write and revise Quality Control Standard Operating Procedures * Supply Quality Control data ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Maintain required training and training records and provide training to qualify other associates ... Write and revise Quality Control Standard Operating Procedures * Supply Quality Control data ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Maintain required training and training records and provide training to qualify other associates ... Write and revise Quality Control Standard Operating Procedures * Supply Quality Control data ...

MW Industries

Quality Control Coordinator

Fairfield, NJ

$20.25 - $27.75/hr

JOB SUMMARY The Quality Control Coordinator provides administrative, organizational, and continuous ... Associate Degree in Business Administration, Manufacturing, Quality, or related field preferred.

MW Industries

Quality Control Coordinator

Fairfield, NJ · On-site

$20.25 - $27.75/hr

JOB SUMMARY The Quality Control Coordinator provides administrative, organizational, and continuous ... Associate Degree in Business Administration, Manufacturing, Quality, or related field preferred.

Adecco

Quality Control I

Piscataway, NJ

$26.51/hr

Adecco Healthcare and Life Sciences is hiring for a Quality Control position in Piscataway, NJ ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Corbion

Quality Control Technician

Totowa, NJ

$24 - $25/hr

The Quality Control Technician, based at the Totowa, NJ plant, reports to the Quality Control ... Associate's Degree in Chemistry, Bio-Chemistry, Chemical Engineering, Biology or Microbiology

corbion

Quality Control Technician

Totowa, NJ · On-site

$24 - $25/hr

The Quality Control Technician, based at the Totowa, NJ plant, reports to the Quality Control ... Associate's Degree in Chemistry, Bio-Chemistry, Chemical Engineering, Biology or Microbiology

Corbion

Quality Control Technician

Totowa, NJ · On-site

$24 - $25/hr

The Quality Control Technician, based at the Totowa, NJ plant, reports to the Quality Control ... Associate's Degree in Chemistry, Bio-Chemistry, Chemical Engineering, Biology or Microbiology

Medline

Supv QC

Tinton Falls, NJ · On-site

$79K - $119K/yr

Job Summary Oversee and manage the Quality Control functions and personnel at designated ... PREFERRED QUALIFICATIONS · Education Associates degree or technical certification preferred.

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Quality Control Associate information

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How much do quality control associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for quality control associate in New Jersey is $25.85, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $31.49 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

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

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in New Jersey?

The most popular types of Quality Control jobs in New Jersey are:

What cities in New Jersey are hiring for Quality Control Associate jobs?

Cities in New Jersey with the most Quality Control Associate job openings:

What are popular job titles related to Quality Control Associate jobs in NJ?

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

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $53,769 per year, or $25.9 per hour.

Quality Control Analyst

Cellares

Bridgewater, NJ • On-site

$90K - $210K/yr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC testing according to Standard Operating Procedures (SOPs).  This role supports the day-to-day operations within the Quality Control group via execution of analytical testing. This includes but is not limited to in-process testing, lot release testing, stability testing, and raw material testing. All activities are all performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures.
 
This role will be a hands-on resource reporting to the Senior Director, Quality Control Bioanalytics.  
 
Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
  • Conduct routine and non-routine analytical, biochemical, and/or biological analysis such as, in-process materials, raw materials, finished goods, or stability samples
  • Work with cell therapy products and associated assays (dPCR, qPCR, cell-based potency assays, proliferation assays, ELISA, flow cytometry assays, etc.)
  • Perform timely and accurate peer review of analytical test results/reports
  • Prepare COA/COT for testing performed
  • Identify discrepancies, initiate and investigate OOS/OOT results for phase 1 and phase 2
  • Initiate and investigate deviations related to quality control
  • Compile and review data to ensure accuracy and regulatory compliance
  • Support development for specifications and justification of specifications
  • Participate in validation and technical transfer of analytical methods commensurate with experience
  • Write and revise test methods
  • Maintain required training and training records and provide training to qualify other associates
  • Participate in internal assessments and audits as required
  • Support equipment validation, calibration, maintenance, and troubleshooting
  • Write method validation protocol/reports and other documentation such as test reports
  • Write stability protocol and stability reports
  • Write and revise Quality Control Standard Operating Procedures
  • Supply Quality Control data necessary for regulatory submissions
  • Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc.
  • Assist in general upkeep of the laboratory and maintain a clean work environment
  • Perform other duties as assigned
Requirements
  • Bachelor's degree in a science discipline required, or comparable experience
  • 2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment, is preferred
  • Prior experience related to method development/validation
  • Prior experience with immune cell phenotyping by multicolor flow cytometry, dPCR, qPCR, cell-based potency and other cell therapy related assays is preferred
  • Knowledge of pharmaceutical cGMP (US and EU) is preferred
  • Must have excellent verbal, written, interpersonal, and organizational and communication skills
  • Must be able to commute to Bridgewater, New Jersey
  • Self-awareness, integrity, authenticity, and a growth mindset
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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