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Quality Control Manager Jobs in Amherst, MA (NOW HIRING)

Viant

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

... 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 ...

medplast

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

... 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 ...

medplast

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

... 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 ...

TAD PGS, Inc.

Quality Inspector

Enfield, CT · On-site

$43K - $47K/yr

Practical experience working with quality management systems (AS9100, ISO9001, NADCAP) This position requires access to technologies and hardware subject to US national security-based export control ...

James Hardie

Quality Coordinator

Westfield, MA · On-site

$79K - $99K/yr

The position promotes disciplined quality management practices aligned with ISO 9001 principles such as process control, risk-based thinking, document control, corrective action, and continual ...

New

James Hardie

Quality Coordinator

Westfield, MA · On-site

$79K - $99K/yr

The position promotes disciplined quality management practices aligned with ISO 9001 principles such as process control, risk-based thinking, document control, corrective action, and continual ...

New

PCX Aerosystems

Quality Inspector

Enfield, CT · On-site

... Control Req Number QUA-25-00017 Position Quality Inspector Close Date Post Internal Days 0 Number of Openings 1 Exempt/Non-Exempt Non-Exempt Hiring Manager(s) This position is currently accepting ...

Valence

Quality Manager

West Springfield, MA · On-site

$90K - $110K/yr

This will include: a) Reviewing the entire quality system and processes and making changes as necessary. b) Establish/maintain and manage process improvement metrics to ensure a reduction in customer ...

Palmer Foundry

Quality Inspector

Palmer, MA · On-site

$20/hr

Dependability - Follows instructions, responds to management direction; takes responsibility for ... Basic Requirements: * 1 - 3 years of quality control experience, ideally in metal casting, die ...

MasTec Industrial

Project Controls Manager

Springfield, MA · On-site

$150K - $200K/yr

This role provides oversight, training, and governance of cost control processes to ensure accuracy ... We're committed to delivering quality, safety, and value at every project phase, from concept to ...

aeis llc

Asphalt Inspector

Springfield, MA · On-site

Work closely with Project Managers, Engineers, and QA/QC Specialists * Contribute to lessons-learned discussions and workflow improvements What We're Looking For Must Haves * NICET Level II Highway ...

Brooks Construction LLC

Project Manager

Enfield, CT · On-site

Develops and adheres to the budget, timeline, and quality control plan. Collaborates with ... Manage project budgets, cost tracking, and change orders. * Oversee subcontractor agreements ...

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All JobsQuality Control JobsQuality Control Manager JobsQuality Control Manager Jobs in Amherst, MA

Quality Control Manager information

See Amherst, MA salary details

$30K

$80.1K

$127.5K

How much do quality control manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for quality control manager in Amherst, MA is $80,093.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,600.00 and $98,500.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

What are the key skills and qualifications needed to thrive as a quality control manager, and why are they important?

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
More about Quality Control Manager jobs
What are the most commonly searched types of Quality Control jobs in Amherst, MA? The most popular types of Quality Control jobs in Amherst, MA are:
What job categories do people searching Quality Control Manager jobs in Amherst, MA look for? The top searched job categories for Quality Control Manager jobs in Amherst, MA are:
What cities near Amherst, MA are hiring for Quality Control Manager jobs? Cities near Amherst, MA with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Amherst, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $80,093 per year, or $38.5 per hour.

Quality Engineer

Viant

Brimfield, MA • On-site

$70K - $95K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 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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