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Quality Control Associate Jobs in Norwood, MA (NOW HIRING)

Rust-Oleum

Mgr/Quality Control

Attleboro, MA

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

New

Kop-Coat, Inc.

Mgr/Quality Control

Attleboro, MA

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

New

Rust-Oleum

Mgr/Quality Control

Attleboro, MA · On-site

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

New

Tremco Construction

Mgr/Quality Control

Attleboro, MA · On-site

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

New

Adecco

Quality Control Technician

Sutton, MA

$18 - $23/hr

Quality Control Technician Location: Sutton, MA Pay Range: $19 - $23 per hour Schedule: Monday ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

Quality Control Technician

Sutton, MA

$18 - $23/hr

Quality Control Technician Location: Sutton, MA Pay Range: $19 - $23 per hour Schedule: Monday ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Norwood, MA

Quality Control Associate information

See Norwood, MA salary details

$13

$28

$43

How much do quality control associate jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for quality control associate in Norwood, MA is $28.77, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $35.05 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 Norwood, MA?

The most popular types of Quality Control jobs in Norwood, MA are:

What cities near Norwood, MA are hiring for Quality Control Associate jobs?

Cities near Norwood, MA with the most Quality Control Associate job openings:

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Norwood, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 84% In-person, 8% Hybrid, and 8% Remote job distribution, with an average salary of $59,837 per year, or $28.8 per hour.

QC Associate, Raw Materials

Norwood, MA • On-site

JMD Technologies Inc.
See more jobs at JMD Technologies Inc.external

$35 - $40/hr

Other

Posted 5 days ago

Job description

Title : QC Associate, Raw Materials I, II

Location: Norwood, MA (On-Site)

Employment Type: Contract

Status: Accepting Candidates


About the Role

The Quality Control Associate will support cGMP QC testing for raw materials, drug substances, and finished products at a manufacturing facility and affiliated contract organizations.

This role includes executing and troubleshooting analytical methods, supporting method transfers and qualification activities, and ensuring compliance with cGMP standards.


Key Responsibilities

QC Testing & Laboratory Support

  • Execute QC molecular biology and Bioassay methods, including mammalian cell-based potency, QPCR, sequencing, and protein analysis
  • Assist in troubleshooting equipment and assay issues
  • Perform reagent preparation, equipment maintenance, housekeeping, and logbook reviews
  • Establish and maintain a safe laboratory working environment


Documentation & Quality Systems

  • Write, revise, and maintain SOPs, protocols, and reports
  • Assist in execution of quality records, including investigations, change controls, and CAPAs
  • Ensure compliance with cGMP documentation and regulatory guidelines
  • Support training as assigned


Compliance & Continuous Improvement

  • Maintain mandatory training and assigned tasks
  • Provide support during audits
  • Collaborate on continuous improvement initiatives
  • Perform additional duties as assigned


Qualifications

BA/BS Degree

  • STEM degree with 3–5 years of experience in a cGMP laboratory setting


Hands-on experience with:

  • Mammalian cell culture
  • Cell-based and potency assays
  • ELISA
  • Molecular biology
  • Protein analysis


Preferred Qualifications

  • Method development/qualification experience with molecular biology, cell-based assays, or protein analysis methods
  • Experience with aseptic techniques and general laboratory instrumentation
  • Experience with pH meters, balances, and pipettes
  • Ability to prepare reagents and pipette small volumes
  • Experience working in a Biological Safety Cabinet
  • Laboratory equipment calibration and maintenance experience
  • Ability to work effectively in a fast-paced, cross-functional matrix environment
  • Familiarity with FDA, EU, ICH guidelines, and regulations


Compensation

  • Level I: $30–$35/hr (0–2 Years Experience)
  • Level II: $35–$40/hr (3–5 years' experience)
  • Norwood, MA – 100% On-Site
  • Monday–Friday, 8:00 AM–5:00 PM
  • 6+ Month Contract

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