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Medical Device Quality Control Jobs in Springfield, MA

Projects Inc.

Quality Inspector

Glastonbury, CT

... medical device, or precision manufacturing environments. * Ability to read and interpret ... Document control and traceability requirements Key Competencies * Attention to detail * Problem ...

PSG Global Solutions

R-D Engineer

Chicopee, MA · On-site

Medical device and design control experience is required. Summary of Position: Coordinate the remediation work for the site while working with and providing mentorship for the DHF remediation ...

UFP Technologies

Production Manager

Chicopee, MA · On-site

UFP is an important link in the medical device supply chain and a valued outsource partner to most ... Initiates and manages quality and cost improvement activities. This position works in collaboration ...

PSG Global Solutions

Assoc R-D Engineer

Chicopee, MA · On-site

Medical device experience preferred. Summary of Position: Support remediation work on assigned ... Prepare full DHF documentation in accordance with relevant internal SOPs and Design Control.

LITRON LLC

Process Engineering Manager

Agawam, MA · On-site

$85K - $115K/yr

Experience leading technical work or teams in aerospace, defense, medical device, RF/microwave, or ... Quality Management * Become familiar with and comply with PacAero's Quality Management System (QMS ...

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Medical Device Quality Control information

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How much do medical device quality control jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for medical device quality control in Springfield, MA is $20.90, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $23.41 per hour, depending on experience, location, and employer.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

What are the key skills and qualifications needed to thrive as a medical device quality control professional?

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What are popular job titles related to Medical Device Quality Control jobs in Springfield, MA?

For Medical Device Quality Control jobs in Springfield, MA, the most frequently searched job titles are:

What job categories do people searching Medical Device Quality Control jobs in Springfield, MA look for?

The top searched job categories for Medical Device Quality Control jobs in Springfield, MA are:

What cities near Springfield, MA are hiring for Medical Device Quality Control jobs?

Cities near Springfield, MA with the most Medical Device Quality Control job openings:

Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control job openings in Springfield, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $43,475 per year, or $20.9 per hour.

Quality Inspector

Glastonbury, CT

Projects Inc.
Aerospace Product and Parts Manufacturing • 51 - 200 employees
Learn more about Projects Inc.external

Full-time

Re-posted 14 days ago

Job description

Description

Quality Inspector Job Description

Projects Inc. is seeking a Quality Inspector to join our Quality team. For more than 50 years, Projects Inc. has manufactured complex precision-machined components for the aerospace and power systems industries. Reporting directly to the Quality Manager, the Quality Inspector is responsible for ensuring that machined and assembled products meet all customer, regulatory, and company quality requirements prior to shipment.

The Quality Inspector is responsible for verifying that aerospace components, assemblies, and finished products meet engineering specifications, customer requirements, and industry standards. This position performs detailed inspections throughout the manufacturing process and ensures compliance with AS9100, FAA, customer, and regulatory requirements while promoting product quality and safety.


Inspection Activities

  • Perform dimensional, visual, and functional inspections of machined components, assemblies, and materials.
  • Conduct first article, in-process, and final inspections.
  • Utilize precision measuring equipment including micrometers, calipers, gauges, and specialized inspection tools.
  • Read and interpret engineering drawings, blueprints, GD&T requirements, specifications, and quality plans.
  • Review material certifications and supplier documentation for accuracy and compliance.
  • Collaborate with engineering, manufacturing, and supply chain teams to resolve quality issues.
  • Obtain and maintain various certifications as required.
  • Conduct First Article Inspections (FAI) in accordance with AS9102 requirements.
  • Verify material certifications, process certifications, and traceability documentation.

Quality Assurance

  • Identify, document, and report nonconforming materials and products.
  • Generate and maintain inspection records and quality documentation.
  • Participate in root cause investigations and corrective action activities (RCCA).
  • Ensure compliance with company quality procedures and aerospace standards.

Documentation & Compliance

  • Review work orders, travelers, inspection plans, and quality records for completeness and accuracy.
  • Maintain accurate inspection reports and records in accordance with regulatory and customer requirements.
  • Support customer, regulatory, and internal quality audits.
  • Ensure adherence to AS9100 and customer-specific requirements.

Measurement & Testing

  • Utilize precision inspection equipment including:
  • Calipers
  • Micrometers
  • Height gauges
  • Dial indicators
  • Optical comparators
  • Coordinate Measuring Machines (CMM)
  • Surface plate inspection equipment
  • Verify dimensional, visual, and functional requirements of products.
  • Monitor calibration status of inspection equipment.

Continuous Improvement

  • Assist in identifying process improvement opportunities.
  • Support quality initiatives aimed at reducing defects and improving efficiency.
  • Participate in quality meetings and problem-solving teams.
  • Promote a culture of safety, quality, and continuous improvement.


Requirements

Required Qualifications

  • High school diploma or GED required.
  • Technical certification or associate degree in Quality, Manufacturing, Engineering Technology, or related field preferred.
  • Minimum 3 to 5 years or more of inspection experience in aerospace, aviation, defense, medical device, or precision manufacturing environments.
  • Ability to read and interpret engineering drawings, blueprints, and technical specifications.
  • Knowledge of Geometric Dimensioning and Tolerancing (GD&T).
  • Proficient in the use of precision measuring instruments.
  • Strong attention to detail and accuracy.

Preferred Qualifications

  • ASQ Certified Quality Inspector (CQI) certification.
  • Experience with AS9100 quality systems.
  • Experience performing First Article Inspections (AS9102).
  • CMM operation and programming experience.
  • Familiarity with FAA, EASA, military, or defense industry requirements.
  • Experience using ERP and Quality Management Systems (QMS).

Technical Skills

  • Blueprint and engineering drawing interpretation
  • GD&T interpretation
  • Precision measurement techniques
  • First Article Inspection (AS9102)
  • Non-conformance reporting
  • Root cause analysis support
  • Microsoft Office applications
  • Quality Management Systems (QMS)
  • Document control and traceability requirements

Key Competencies

  • Attention to detail
  • Problem-solving skills
  • Integrity and accountability
  • Communication skills
  • Time management
  • Ability to work independently
  • Team collaboration
  • Commitment to safety and quality

Physical Requirements

  • Ability to stand, walk, bend, and lift up to 40 pounds.
  • Manual dexterity required for handling small precision components.
  • Ability to perform detailed visual inspections.
  • Ability to work in both office and manufacturing environments.

Working Conditions

  • Manufacturing, production, laboratory, and inspection environments.
  • May require use of personal protective equipment (PPE).
  • Occasional overtime may be required to meet production schedules and customer deadlines.

Acknowledgments:

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their manager.

Projects Incorporated is an Equal Opportunity Employer and does not discriminate based on race, ancestry, color, religion, sex, age, marital status, sexual orientation, national origin, medical condition, disability, veteran status, gender identity, or any other basis protected by law.


Drug-Free and Alcohol-Free Workplace

In compliance with the Drug-Free Workplace Act of 1988, Projects is committed to providing a safe, quality-oriented, and productive work environment. Alcohol and drug use and abuse pose a threat to the health and safety of our employees, to the security of our equipment, facilities, and product quality. 

For these reasons, Projects is dedicated to the elimination of drug and alcohol use and abuse in the workplace.

This policy applies to all employees and all applicants for employment at Projects. Human Resources is responsible for the administration of this policy.

Pre-employment

Applicants being considered for hire must pass a drug test after written acceptance of an offer of employment and before beginning work. Refusal to submit to testing will result in disqualification of further employment consideration.

All applicants are subject to pre-employment drug testing and will be assigned to a testing facility designated by Projects and directed to provide a urine specimen. Collected specimens will be sent to a federally certified laboratory and tested for evidence of marijuana, cocaine, opiates, amphetamines, PCP, benzodiazepines, methadone, methaqualone, propoxyphene use, and specimens may be tested for other illegal drug(s)..  



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