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Quality Control Associate Jobs in Springfield, MA

Viant

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

... associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses ...

medplast

Quality Engineer

Brimfield, MA

$70K - $95K/yr

... associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses ...

medplast

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

... associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses ...

medplast

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

... associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses ...

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

Quality Control Associate information

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$25

$38

How much do quality control associate jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for quality control associate in Springfield, MA is $25.37, according to ZipRecruiter salary data. Most workers in this role earn between $18.46 and $30.91 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 Springfield, MA? For Quality Control Associate jobs in Springfield, MA, the most frequently searched job titles are:
What cities near Springfield, MA are hiring for Quality Control Associate jobs? Cities near Springfield, MA with the most Quality Control Associate job openings:
Quality Control Associate jobs near you
Quality Engineer

Quality Engineer

Viant

Brimfield, MA • On-site

$70K - $95K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 days ago

Job description

New employees are eligible for the following benefits effective date of hire!
  • Full Medical, Dental & Vision, 401(k), effective on your 1st day
  • Generous paid time off benefits and 10 paid Holidays
  • Growth Opportunities
  • On-Demand Pay: Access your pay as soon as you have earned it!
  • We offer market competitive compensation. Potential salary range for this role is $70,000-95,000 annual wage. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.

Description
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance.
Responsibilities
  • Adheres to Viant Core Beliefs and all safety and quality requirements including, but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug Administration (FDA) regulations, Company policies and operating procedures, and other regulatory requirements.
  • Supports regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
  • Monitors manufacturing of assigned products, assuring compliance with DMR while providing deviation/waiver guidance and assuring complete and correct Device History Records are maintained.
  • Leads and implements various product and process improvement methodologies.
  • Review the adequacy and correctness of changes to Bill of Materials (BOM's), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
  • Leads in the completion and maintenance of risk analysis.
  • Leads generation and completion of protocols and reports for test method validations.
  • Interfaces with Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
  • Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval and implementation of Incoming, In-Process and Final Inspection procedures.
  • Ensures that the disposition of non-conforming materials meet all necessary regulatory requirements and assure adequacy of corrective actions to prevent re-occurrence.
  • Effectively communicate and interact with customers.
  • Leads and manage complaint investigations.
  • Acts as a lead in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root causes analysis.
  • Assists with product transfers.
  • Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
  • Coordinates and leads the preparation of Quality Plans, including inspection, test and gauge requirements for new product introductions
  • This position may provide work direction for 3-5 Inspectors/Technicians.
  • Provides support to other quality engineers.
  • Performs other functions as required.

The successful candidate will:
  • Manage a heavy workload while maintaining accuracy
  • Identify potential roadblocks and provide innovative solutions
  • Operate with a high level of integrity and professionalism
  • Committed to and accountable for achieving goals and objectives

Education/Certification
  • Bachelor's Degree in Engineering or related field required or 2 - 5 years of experience working in a quality engineering role within a regulated industry.

Experience
  • 2-5 years' experience in medical device or regulated manufacturing

Skills/Competencies
  • Competence in the selection and use of Quality Engineering Tools and Techniques.
  • Strong communication skills and ability to align with key stakeholders
  • Strong working knowledge in the interpretation and application of relevant Domestic and International Regulations and Industry Standards (e.g. FDA 21CRF820, ISO 13485:2016; MDSAP; ISO14971, QSR, MDD, TGA etc.)
  • Proficient in Microsoft Office and Minitab

Travel
  • Less than 10%

Physical Requirements
  • Light work: Exerting up to 20 pounds of force occasionally, and/or up to 10 pounds of force frequently, and/or lift, carry, push, pull, or move objects

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