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Quality Assurance Incoming Inspector Jobs in Randolph, MA

Kettle Cuisine

QA Technician

Lynn, MA

$18 - $21/hr

Job Summary The Food Manufacturing Quality Assurance Line Technician is a full-time position ... Testing and Inspection: Performing routine tests on the environment and food contact surfaces of ...

Kettle Cuisine

QA Technician

Lynn, MA

Job Summary The Food Manufacturing Quality Assurance Line Technician is a full-time position ... Testing and Inspection: Performing routine tests on the environment and food contact surfaces of ...

Trexon

QC Inspector

Chelsea, MA

$18 - $25/hr

Identify and log incoming shelf-life material. Assist when needed with shelf-life material audits. * Perform in-process inspections based on schedule issued by Quality Manager. * When required ...

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Quality Assurance Incoming Inspector information

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$13

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$39

How much do quality assurance incoming inspector jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for quality assurance incoming inspector in Randolph, MA is $23.28, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $26.25 per hour, depending on experience, location, and employer.

What does a quality assurance incoming inspector do?

A Quality Assurance Incoming Inspector is responsible for inspecting and verifying the quality of raw materials, components, or products as they arrive from suppliers before they are used in the manufacturing process. They check for defects, compliance with specifications, and adherence to quality standards. Their role helps ensure that only materials that meet company criteria are used, which helps prevent production issues and maintains product quality. Inspectors typically use measuring tools, review documentation, and may create reports on their findings.

What are the key skills and qualifications needed to thrive as a quality assurance incoming inspector?

To thrive as a Quality Assurance Incoming Inspector, you need strong attention to detail, knowledge of quality control standards, and often a background in manufacturing or a related technical field. Familiarity with measurement tools (calipers, micrometers), inspection software, and sometimes certifications such as ASQ Certified Quality Inspector are typically required. Excellent documentation skills, problem-solving abilities, and clear communication are essential soft skills in this role. These skills and qualifications ensure accurate verification of incoming materials, support compliance with quality standards, and help prevent defects in the manufacturing process.

What are some typical challenges faced by quality assurance incoming inspectors when evaluating new materials or components?

Quality Assurance Incoming Inspectors often encounter challenges such as identifying subtle defects in large batches, understanding complex technical specifications, and keeping up with evolving quality standards. They must work closely with suppliers and internal teams to resolve discrepancies and ensure that all incoming materials meet strict requirements. Managing time effectively to inspect high volumes without sacrificing accuracy is also a critical aspect of the role.

What is the difference between Quality Assurance Incoming Inspector vs Quality Control Inspector?

AspectQuality Assurance Incoming InspectorQuality Control Inspector
Primary FocusPrevent defects by inspecting incoming materialsIdentify defects in finished products or during production
Work EnvironmentReceiving areas, supplier sites, warehousesProduction lines, testing labs, final inspection areas
CertificationsISO 9001, ASQ certifications often preferredQuality control certifications, sometimes ASQ Certified Quality Inspector
Employer & Industry UsageManufacturing, aerospace, automotive, electronicsManufacturing, consumer goods, electronics, automotive

While both roles focus on quality, the Quality Assurance Incoming Inspector emphasizes preventing defects by inspecting incoming materials, whereas the Quality Control Inspector concentrates on identifying defects during or after production. Understanding these differences helps employers and job seekers target the right skills and certifications for each position.

What are popular job titles related to Quality Assurance Incoming Inspector jobs in Randolph, MA?

For Quality Assurance Incoming Inspector jobs in Randolph, MA, the most frequently searched job titles are:

What job categories do people searching Quality Assurance Incoming Inspector jobs in Randolph, MA look for?

The top searched job categories for Quality Assurance Incoming Inspector jobs in Randolph, MA are:

What cities near Randolph, MA are hiring for Quality Assurance Incoming Inspector jobs?

Cities near Randolph, MA with the most Quality Assurance Incoming Inspector job openings:

Quality Assurance Incoming Inspector jobs near you
Infographic showing various Quality Assurance Incoming Inspector job openings in Randolph, MA as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $48,430 per year, or $23.3 per hour.

Quality Assurance Specialist

Nova Biomedical Corporation

Billerica, MA โ€ข On-site

$77K - $86K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

Job description

Nova Biomedical: One Global Brand. One Vision. Together under one name.
Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets.
Job Summary:
The Quality Assurance (QA) Specialist supports the effectiveness, compliance, and continual improvement of the Quality Management System (QMS) by coordinating key quality processes. This role works cross-functionally to maintain an inspection-ready QMS, ensure compliance with regulatory and quality requirements, support implementation of external requirements, and drive continuous improvement initiatives that enhance overall quality system performance and operational effectiveness.
Responsibilities:
  • Support the maintenance and improvement of the QMS to ensure compliance with regulatory requirements, industry standards, and internal procedures
  • Manage the Documents of External Origin program, including monitoring, review, distribution, maintenance, and impact assessments of applicable regulations and standards
  • Review quality records for completeness, accuracy, and compliance with Good Documentation Practices (GDP) and retention requirements
  • Provide administrative support for equipment calibration and preventive maintenance programs, including tracking and reporting
  • Support preparation and execution of external audits and inspections, including record coordination and evidence retrieval
  • Conduct internal quality audits and support closure of findings and actions
  • Initiate, revise, and review controlled documents including SOPs, work instructions, forms, and templates
  • Prepare and review Engineering Change Orders (ECOs), Manufacturing Variances (MVs), and other controlled changes
  • Support quality system processes such as CAPA, nonconformance, investigations, and shipping holds
  • Track deliverables, actions, and due dates to ensure timely completion of quality activities
  • Identify and escalate documentation gaps, procedural issues, and compliance concerns
  • Support employee training related to QMS procedures and compliance
  • Collaborate with cross-functional teams including Manufacturing, Engineering, Regulatory Affairs, Quality Control, Supplier Quality, Supply Chain, Technical Support, and R&D
  • Perform other quality system and compliance-related duties as assigned

Experience Requirements:
  • Bachelor's degree in a scientific, technical, business, or related discipline preferred
  • 3๏ฟฝ5+ years of experience in Quality Assurance, Quality Systems, Regulatory Compliance, Document Control, or a related function in a regulated industry
  • Experience supporting QMS, audits, change control, and compliance activities preferred
  • Experience within medical device, IVD, pharmaceutical, biotechnology, or similar regulated industries preferred
  • Equivalent combination of education and experience may be considered

Physical Requirements and Working Conditions:
  • Comfort with working at a computer for extended periods.
  • Capacity to lift and carry up to [25๏ฟฝ50] pounds as required
  • Able to communicate effectively via phone, video, and written communication.
  • Occasional need to move about the office to access meetings or resources.

Why Work for Nova Biomedical
  • Flexible Medical, Dental, & Vision Coverage
  • Competitive 401k company match
  • Bonus Program, Generous PTO and paid holidays
  • Generous Tuition reimbursement
  • Hybrid and flexible work arrangements
  • Professional development, engagement and events
  • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
  • Company subsidized cafeteria in our Waltham, MA office

Work Location: Hybrid work schedule on-site in Billerica, Manning Rd
Targeted Salary Range: $77,000 - $86,000/year.
Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate's experience and may vary based on individual factors such as location, skills, and education.
About the company
At Nova Biomedical, we're not just building instruments, we're powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.
Our integration brings together more than 70 years of scientific excellence with Nova's cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we're setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.
With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we're building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.
Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you'll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health.
Explore what's next with us at novabiomedical.com
EEO Statement:
Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
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