1

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

Inventory Control Associate

Sayreville, NJ · On-site

$17.75 - $21.75/hr

Description * We are looking for an hourly Inventory Control Associate. Schedule is Monday to ... Work in accordance with all company policies and procedures regarding safety, quality, product ...

New

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 ...

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 ...

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 ...

The Scientist, Quality Control conducts routine and non-routine analysis, including but not limited ... Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal ...

The Scientist, Quality Control conducts routine and non-routine analysis, including but not limited ... Production Associate Roles : Must have visual acuity of 20/20 (corrected or uncorrected) and normal ...

The Scientist, Quality Control conducts routine and non-routine analysis, including but not limited ... Production Associate Roles : Must have visual acuity of 20/20 (corrected or uncorrected) and normal ...

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.

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. Medline ...

next page

Showing results 1-20

Quality Control Associate information

See Edison, NJ salary details

$11

$26

$39

How much do quality control associate jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for quality control associate in Edison, NJ is $26.36, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $32.12 per hour, depending on experience, location, and employer.

What is a QC Associate job description?

A Quality Control (QC) Associate is responsible for inspecting and testing products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like measurement instruments and quality management systems. The role typically requires attention to detail, knowledge of quality procedures, and adherence to safety protocols.

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, and why are they important?

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.

Which pays more, QA or QC?

Quality Assurance (QA) and Quality Control (QC) roles often have similar pay scales, but QA positions typically offer higher salaries due to their focus on process improvement and prevention. Factors such as industry, experience, certifications, and location can influence compensation for both roles.

What do quality control associates do?

Quality control associates inspect products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or production environments to identify defects and ensure product consistency.

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.

Is QC a high paying job?

The salary for a Quality Control Associate varies depending on industry, experience, and location, but it is generally considered an entry-level to mid-level position with moderate pay. Higher salaries are often associated with advanced certifications, specialized skills, or supervisory roles within quality control departments.
What are popular job titles related to Quality Control Associate jobs in Edison, NJ? For Quality Control Associate jobs in Edison, NJ, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Edison, NJ look for? The top searched job categories for Quality Control Associate jobs in Edison, NJ are:
What cities near Edison, NJ are hiring for Quality Control Associate jobs? Cities near Edison, NJ with the most Quality Control Associate job openings:
Infographic showing various Quality Control Associate job openings in Edison, 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 $54,830 per year, or $26.4 per hour.
Associate, QC Analytical, Cell Therapy

Associate, QC Analytical, Cell Therapy

Bristol Myers Squibb

Summit, NJ • On-site

$36.90 - $44.71/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago


Bristol Myers Squibb rating

8.1

Company rating: 8.1 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

33rd of 74 rated pharmaceutical


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

The Associate, QC Analytical is responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.

Shift Available:

  • Sunday - Wednesday, Onsite Day Shift, 6:30 a.m. - 4:30 p.m.

Responsibilities:

  • Perform routine testing of in-process, final product, and stability samples.

  • May review GMP documentation and perform data verification.

  • Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.

  • May train analysts on general job duties.

  • Perform other tasks as assigned.

Knowledge & Skills:

  • Ability to accurately and completely understand and follow procedures.

  • Apply scientific principles to analytical testing and the proper use of laboratory equipment.

  • Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.

  • Attention to detail and demonstrated organizational skills.

  • Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Basic Requirements:

  • Bachelor's degree preferred in science. Associate's degree with equivalent combination of education and work experience may be considered.

  • 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.

  • Pipetting experience required.

  • Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.

Preferred Requirements:

  • Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.

  • Prior specimen preparation experiences ideal.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Summit West - NJ - US: $36.90 - $44.71per hour

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

  • Health Coverage: Medical, pharmacy, dental, and vision care.

  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:

Paid Time Off

  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)

  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1603824 : Associate, QC Analytical, Cell Therapy

What Bristol Myers Squibb employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Bristol-Myers Squibb logo

About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US