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

Integra LifeSciences

Lead Quality Inspector

Plainsboro, NJ · On-site

$26.21 - $35.38/hr

The lead associate is responsible for performing and/or scheduling quality assurance inspections on ... Prepare the QC Inspection schedule to ensure that all manufacturing areas are covered in order to ...

Integra LifeSciences

Lead Quality Inspector

Plainsboro, NJ · On-site

$26.21 - $35.38/hr

The lead associate is responsible for performing and/or scheduling quality assurance inspections on ... Prepare the QC Inspection schedule to ensure that all manufacturing areas are covered in order to ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Howell, NJ

Quality Control Associate information

See Howell, NJ salary details

$11

$25

$38

How much do quality control associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for quality control associate in Howell, NJ is $25.57, according to ZipRecruiter salary data. Most workers in this role earn between $18.61 and $31.15 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 Howell, NJ?

The most popular types of Quality Control jobs in Howell, NJ are:

What cities near Howell, NJ are hiring for Quality Control Associate jobs?

Cities near Howell, NJ with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Howell, NJ as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $53,180 per year, or $25.6 per hour.

Senior Associate Scientist, QC Testing - Raw Materials & Compendial

WuXi Biologics

Cranbury, NJ • On-site

$54K - $87K/yr

Full-time

Posted 17 days ago

Job description

Job Title - QC Senior Associate Scientist - Micro/RM/Compendial Testing and Sampling
Work Location - Cranbury, NJ
Job Summary
The QC Micro/RM/Compendial Senior Scientist is responsible for the quality and on-time completion of microbiology/raw material/compendial testing and sampling. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates good oral and written communication skills and actively contributes to timely training, report generation and good GMP documentation and archival.
Job Functions
  • Understand GMP and follow instructions on the documents.
  • Perform microbiology/raw material/compendial testing including but not limited to FTIR, pH, Color, Clarity, visible and subvisible particles, osmolarity, bioburden, endotoxin, CCIT, etc.
  • Able to follow and conduct EM/water/gas sampling in cleanroom areas in/between the various building sites in Cranbury or other US sites (when needed).
  • Need to support RM sample sampling and its transporting needs in/between the various building sites in Cranbury or other US sites (when needed).
  • Management of raw material, EM monitoring samples, raw material sampling room, sample storage room and regulatory retain sample room, etc., and ensuring the sampling process and storage of raw material samples or incubation of EM samples are under conducted properly and within control (when needed)
  • Support reagents/consumables inventory management to ensure consistent QC EM operation needs.
  • Record and organize experimental data in accordance with "Good Document Management Practices" to ensure data integrity.
  • Ensure compliance with training, preparation, documentation and general lab maintenance requirements for Industry Standards and/or Regulations.
  • Assist in preparing or executing validation documents to support new materials, process changes and qualifications.
  • Maintains laboratory notebooks and worksheets for QC tasks as required.
  • Able to work at weekend when needed.
  • Support shift work when needed.
  • Any other duties assigned by the supervisor (when applicable).

As Subject Matter Expert:
  • Generate documents such as SOPs, analytical methods, and On The Job training and trains junior staff on methods.
  • Optimize methods to improve efficiency while adhering to Quality Control standards.
  • Troubleshoot any issues on assays, instruments, or reagents.
  • Investigate any OOS/OOT and atypical results and laboratory investigations, conduct root cause analysis, and implement CAPA.
  • Attend internal and external meetings and present data summary, investigation results, or trending analysis to project teams or clients.
  • Proactively respond to and participate in scheduled audits and able to defend methodologies to auditors.

Job Requirement
Technical Skills / Knowledge:
  • Candidate must possess willingness to learn analytical and QC operations of pharmaceutical industry, understand current regulations and industry trends of biologics product development, characterization and manufacturing testing requirement including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance.
  • Basic familiarity with analytical instruments and methodologies, such as TOC, conductivity meter is preferred but not mandatory.
  • Basic experience with software and information systems (eg. Empower, TrackWise, Master Control, LES, lab notebook and preferably LIMS). Ability to adapt between strategic and tactical thinking/planning and manage multiple priorities to achieve department and site objectives.
  • Ability to understand technical data

Problem Solving:
  • Experience in planning and ability to solve QC technical and operation problems.
  • Be able to raise issues immediately to supervisor and work with supervisor when in doubt.

Communication Skills:
  • Proficiency in English is required. Good communications skills (verbal, written, and presentation skills).
  • Effectively exchange information or discuss clearly framed issues or ideas with colleagues.

Education and Experience:
  • Full-time undergraduate degree or above, majoring in biology, chemical engineering, chemistry, pharmacy or related majors.
  • Bachelor's degree: 9+ years of experience in the professional field
  • Master's degree: 7+ years of experience in the professional field
  • PhD: 2+ years of experience in the professional field

The anticipated salary range for this position is $54,700 to $87,500
Job description does not intend to list all the duties and responsibilities assigned to this position. Employees holding this position are required to perform other job-related duties/responsibilities based on their expertise and company business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

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