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

Quality Control Technician

NJ · On-site

$19.75 - $25.25/hr

Apply best practices from within the field of quality to ensure that the materials, components ... Associate's degree, preferred * Over 5 years of equivalent experience in a related field ...

Quality Control Technician

North Brunswick, NJ · On-site

$19.75 - $25.25/hr

Apply best practices from within the field of quality to ensure that the materials, components ... Associate's degree, preferred * Over 5 years of equivalent experience in a related field ...

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

Job Title - Scientist I, QC Work Location - Cranbury, NJ Job Summary: We are seeking a self ... Ability to lead a team of Associate Scientist and Scientist to perform tasks. The anticipated ...

Assistant Manager, Quality Control

NJ · On-site

$66K - $72K/yr

... quality associates 24. Ability to work additional hours as needed PHYSICAL DEMANDS/ ESSENTIAL JOB ... control experience in 24/7 food plant or pharmaceutical setting needed. • HACCP and SQF Systems ...

As our Quality Control Technician you will assure product quality by preparing samples, conducting ... High school diploma or equivalent, Associate's or Bachelor's degree a plus * Some background in ...

As our Quality Control Technician you will assure product quality by preparing samples, conducting ... High school diploma or equivalent, Associate's or Bachelor's degree a plus * Some background in ...

As our Quality Control Technician you will assure product quality by preparing samples, conducting ... High school diploma or equivalent, Associate's or Bachelor's degree a plus * Some background in ...

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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:

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.

Quality Control Technician

LeMaitre

NJ • On-site

$19.75 - $25.25/hr

Full-time

Re-posted 24 days ago


Job description

Overview
The person in this position will uphold and improve the product quality of medical devices manufactured and meet regulatory requirements for compliance. Apply best practices from within the field of quality to ensure that the materials, components, processes, and manufacturing techniques are used to produce high quality and reliable products
Responsibilities
  • Responsible for the proper selection, inspection, and document review of all raw materials, in compliance with approved specifications
  • Inspect items to parameters listed on drawings or quality/material specifications
  • Adeptly read and/or utilizing pin gauges, rulers, micrometers, calipers, microscopes, and other inspection equipment
  • Initiate nonconforming material reports or notices for items not meeting applicable specifications
  • Perform manufacturing audits to ensure that manufacturing procedures are properly followed and that products are tested in accordance with approved test plans
  • Maintain security and integrity of quarantined components and devices
  • Execute activities associated with inspection methods, calibration, maintenance, and record keeping
  • Perform data collection and limited data analysis
  • Coordinate calibration activities as necessary
  • Coordinate and conduct rework and inspection and testing of materials and/or finished goods, as needed, to verify that they meet specifications
  • Assist with administrative functions and supports other department tasks as needed
  • Perform and assist with incoming material receipt and disposition. Notifies Quality and Operations of all nonconformances
  • Issue batch records and production work orders
  • Review production documentation for labeling compliance on current products
  • Review quality and manufacturing records for completion and accuracy
  • Participate in documentation scanning / archiving processes
  • Perform and assist with facility environmental control data collection and ensures conformity is achieved
  • Perform periodic scheduled and unscheduled walk-through review of the manufacturing process, warehouse storage, and associated production areas to ensure that cGMPs are being followed
  • Additional duties, as requested

Qualifications
  • High School Diploma, or equivalent. Associate's degree, preferred
  • Over 5 years of equivalent experience in a related field, preferably in Medical Device
  • Experience in using MS Word, Excel, Power Point and Outlook
  • Strong oral and written communication skills

EEO Statement
In order to provide equal employment and advancement opportunities to all individuals, employment decisions at LeMaitre Vascular will be based on merit, qualifications, and abilities. LeMaitre Vascular does not discriminate in employment opportunities or practices on the basis of race, color, religion, sex, national origin, age, disability, sexual orientation, gender identity, breastfeeding or related medical conditions, religious dress, military or veteran status or any other characteristic protected by law.
This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination, and access to benefits and training.
Applicants with disabilities may contact LeMaitre HR coordinators via telephone, fax, e-mail, and other means to request and arrange for accommodations. If you need assistance to accommodate a disability, you may request an accommodation at any time. Please contact LeMaitre HR at HR@lemaitre.com.