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Quality Control Jobs in Worcester, MA (NOW HIRING)

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) operations across multiple U.S. manufacturing facilities in Waltham, Norwood, and Billerica, Massachusetts ...

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) operations across multiple U.S. manufacturing facilities in Waltham, Norwood, and Billerica, Massachusetts ...

QC Microbiologist II

Hopkinton, MA · On-site

$74K - $85K/yr

QC Microbiologist II in Hopkinton, MA Build your future at Curia, where our work has the power to save lives. The Quality Control Microbiologist II performs quality activities in support of product ...

As part of the Milford site's Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control ...

Job Purpose As the Manager, Quality Control , you will be the departmental owner of inspection workflows, metrology standards, and personnel development. You are responsible for the coordination of ...

QC Microbiologist II

Hopkinton, MA · On-site

$74K - $85K/yr

QC Microbiologist II in Hopkinton, MA Build your future at Curia, where our work has the power to save lives. The Quality Control Microbiologist II performs quality activities in support of product ...

Serve as QC point of contact for CDMOs/CTLs ensuring appropriate quality control oversight of manufacturing campaigns * Ensure CDMOs/CTLs perform release, stability and in‑process testing in ...

Asphalt Quality Control Tech

Westford, MA · On-site

$19.50 - $25/hr

A Quality Control Technician typically performs a wide variety of tasks, transferring from one task to another as the work flow dictates. Key Duties * This position is responsible for controlling the ...

We're looking for a Quality Inspector who takes pride in catching the details and making sure every part leaving our shop meets the required specifications. This is a great opportunity for an ...

We're looking for a Quality Inspector who takes pride in catching the details and making sure every part leaving our shop meets the required specifications. This is a great opportunity for an ...

We're looking for a Quality Inspector who takes pride in catching the details and making sure every part leaving our shop meets the required specifications. This is a great opportunity for an ...

We're looking for a Quality Inspector who takes pride in catching the details and making sure every part leaving our shop meets the required specifications. This is a great opportunity for an ...

Showing results 41-60

Quality Control information

See Worcester, MA salary details

$11

$21

$33

How much do quality control jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for quality control in Worcester, MA is $21.43, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $23.99 per hour, depending on experience, location, and employer.

What is quality control?

Quality control (QC) is a process by which businesses ensure that their products or services meet specific standards of quality. This typically involves systematic inspection, testing, and corrective actions to detect and address defects or inconsistencies. Quality control helps maintain customer satisfaction, comply with regulations, and reduce waste or costly errors. QC can be applied at various stages of production and is essential in industries such as manufacturing, food production, and pharmaceuticals.

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

To thrive as a Quality Control professional, you need keen attention to detail, analytical skills, and a background in science, engineering, or manufacturing, often supported by relevant certifications like Six Sigma or ISO standards. Familiarity with quality management systems (QMS), statistical process control (SPC) software, and inspection equipment is typically required. Strong problem-solving abilities, communication, and teamwork set top performers apart in this role. These skills are crucial to ensure product consistency, prevent defects, and maintain compliance with industry standards.

What are some common challenges faced by quality control professionals and how can they be addressed?

Quality Control professionals often encounter challenges such as maintaining consistency across production batches, adapting to new regulatory standards, and managing tight deadlines without compromising quality. Addressing these challenges requires strong attention to detail, effective communication with production and engineering teams, and continuous learning to stay updated on industry best practices. Many companies support their QC staff with regular training sessions, clear documentation protocols, and collaborative problem-solving meetings to ensure quality standards are upheld.

What is the difference between Quality Control vs Quality Assurance?

AspectQuality ControlQuality Assurance
FocusDetecting defects in products or servicesPreventing defects through process improvements
ActivitiesInspections, testing, samplingProcess audits, standards development
CredentialsOften requires technical training or certifications in testingCertifications like ISO, Six Sigma are common
Work EnvironmentLaboratory, production lines, manufacturingProcess development, documentation, audits

While Quality Control focuses on identifying defects after production, Quality Assurance aims to prevent defects through process improvements. Both roles are essential for maintaining product quality, but they differ in approach and activities.

Is a quality control job physically demanding?

A quality control job can involve physical tasks such as inspecting products, standing for extended periods, and handling materials. The physical demand varies depending on the industry and specific role, but many positions require good attention to detail and manual dexterity. Some roles may also involve lifting or moving objects, so physical fitness can be beneficial.

What do quality control workers do?

Quality control workers inspect products and materials to ensure they meet safety and quality standards. They use tools like measurement devices and follow procedures to identify defects, document issues, and ensure compliance with specifications, often working in manufacturing or production environments. Attention to detail and knowledge of quality standards are essential for this role.

What are the most commonly searched types of Quality Control jobs in Worcester, MA?

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

What are popular job titles related to Quality Control jobs in Worcester, MA?

For Quality Control jobs in Worcester, MA, the most frequently searched job titles are:

What job categories do people searching Quality Control jobs in Worcester, MA look for?

The top searched job categories for Quality Control jobs in Worcester, MA are:

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

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

Infographic showing various Quality Control job openings in Worcester, MA as of August 2026, with employment types broken down into 74% Full Time, 13% Part Time, and 13% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $44,571 per year, or $21.4 per hour.

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago


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 Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) operations across multiple U.S. manufacturing facilities in Waltham, Norwood, and Billerica, Massachusetts, supporting the production of biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD) medical devices, consumables, and reagents.
This role ensures product quality, regulatory compliance, and operational excellence throughout the manufacturing lifecycle, with a strong emphasis on data-driven quality management, statistical monitoring, and continuous improvement. The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies that support FDA medical device requirements, MDSAP, IVDR, ISO 13485, ISO 14971, and other applicable regulatory standards while enabling scalable growth across the organization.
The ideal candidate will be a collaborative leader who partners closely with Manufacturing, Quality Assurance, Regulatory Affairs, R&D, and Operations leadership to drive quality objectives, business expansion, and commercialization goals.
Responsibilities:
  • Lead Quality Control functions across multiple manufacturing and distribution sites within the United States.
  • Establish and maintain enterprise-wide QC strategies, policies, procedures, and performance metrics.
  • Build, develop, and mentor high-performing Quality Control teams while fostering a culture of accountability, compliance, and continuous improvement.
  • Ensure consistency of QC practices, testing methodologies, and inspection standards across all facilities.
  • Drive operational excellence initiatives that improve product quality, efficiency, and scalability.
  • Establish robust systems for collecting, monitoring, analyzing, and reporting product quality and manufacturing performance data.
  • Proactively identify trends, emerging product risks, recurring defects, process shifts, and performance gaps to support continuous improvement.
  • Lead root cause investigations using structured problem-solving methodologies and statistical tools.
  • Analyze quality, yield, reliability, complaint, nonconformance, and production output data to improve product performance and manufacturing capability.
  • Ensure compliance with FDA, MDSAP, IVDR, ISO, and other applicable regulatory requirements and harmonized standards.
  • Oversee the management of documentation, records, test reports, deviations, investigations, CAPAs, and quality metrics.
  • Collaborate with R&D, Supplier Quality, Incoming Inspection, Manufacturing, Manufacturing Engineering, Finished Goods, and Distribution teams to drive quality improvements.
  • Support engineering and manufacturing quality initiatives through the effective use of procedures, processes, quality engineering tools, and data analysis.

Experience Requirements:
  • Bachelor's degree or higher in a technical discipline, preferably within Life Sciences, Chemistry, Medical Technology, or a related field.
  • 5�10+ years of Quality Control management experience within an FDA-regulated medical device, IVD, or reagent manufacturing environment.
  • Strong working knowledge of ISO 13485, ISO 14971, MDSAP, IVDR, and FDA regulations including 21 CFR Part 820.
  • Experience developing product and process trend analyses, nonconformance reduction programs, risk reduction initiatives, cost containment efforts, and executive-level quality reporting.
  • Experience applying product lifecycle risk management principles for IVD medical devices.
  • Experience linking QC trends, nonconformances, complaint investigations, and manufacturing performance data to product risk management activities.
  • Experience with process and equipment validation activities, including authoring and reviewing IQ, OQ, and PQ documentation.
  • Experience authoring Quality Plans and Quality Control Plans.
  • Experience supporting multi-site manufacturing operations.
  • Strong project management, leadership, and team development skills.
  • ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE), ASQ Certified Quality Engineer (CQE), and/or Green Belt Six Sigma certification preferred.

Physical Requirements and Working Conditions:
  • Comfort with working at a computer for extended periods.
  • Capacity to lift and carry up to [25�50] 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: Waltham, MA
Targeted Salary Range: $150,000-$170,000/yr
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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