ZipRecruiter

Log In

1

Senior Quality Control Engineer Jobs in Boston, MA

Nova Biomedical

Sr. QC Manager

Waltham, MA · On-site

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) ... Support engineering and manufacturing quality initiatives through the effective use of procedures ...

NOVA Biomedical GmbH

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

Job Summary The Sr. Quality Control Manager is responsible for leading and scaling Quality Control ... Support engineering and manufacturing quality initiatives through the effective use of procedures ...

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

Job Summary The Sr. Quality Control Manager is responsible for leading and scaling Quality Control ... Support engineering and manufacturing quality initiatives through the effective use of procedures ...

Nova Biomedical

Sr. QC Manager

Waltham, MA · On-site

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) ... Support engineering and manufacturing quality initiatives through the effective use of procedures ...

Nova Biomedical

Sr. QC Manager

Waltham, MA

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) ... Support engineering and manufacturing quality initiatives through the effective use of procedures ...

Exyte

Senior Engineer QA/QC CSA

Boston, MA · On-site

$90 - $120/hr

Discover your exciting role The Senior QA/QC CSA Engineer will be responsible for conducting inspections to ensure that work on a site complies with project design documents, industry standards, and ...

Exyte Group

Senior Engineer QA/QC CSA

Boston, MA · On-site

$47.33/hr

Discover your exciting role The Senior QA/QC CSA Engineer will be responsible for conducting inspections to ensure that work on a site complies with project design documents, industry standards, and ...

MassHousing

Quality Control Specialist

Boston, MA · On-site

$15K/yr

This position reports to the Senior Quality Control Specialist. All positions at MassHousing require a customer service mindset in accordance with our values: Respect, Service, Empathy ...

MassHousing

Quality Control Specialist

Boston, MA · On-site

$74K - $96K/yr

This position reports to the Senior Quality Control Specialist. All positions at MassHousing require a customer service mindset in accordance with our values: Respect, Service, Empathy ...

Nova Biomedical

Senior Quality Engineer

Norwood, MA · On-site

$100K - $135K/yr

Format, manage and maintain Quality Control Plans and PFMEAs for new products to ensure that ... 4+ as a Senior Quality Engineer within an FDA regulated reagents, medical device, or IVD ...

Nova Biomedical

Senior Quality Engineer

Norwood, MA · On-site

$100K - $135K/yr

Format, manage and maintain Quality Control Plans and PFMEAs for new products to ensure that ... 4+ as a Senior Quality Engineer within an FDA regulated reagents, medical device, or IVD ...

Nova Biomedical

Senior Quality Engineer

Norwood, MA

$100K - $135K/yr

Format, manage and maintain Quality Control Plans and PFMEAs for new products to ensure that ... 4+ as a Senior Quality Engineer within an FDA regulated reagents, medical device, or IVD ...

Foundation Medicine

Senior Quality Engineer

Boston, MA

$101K - $126K/yr

The Senior Quality Engineer is responsible for governance, optimization, lifecycle support, and ... The position supports Quality Systems processes including CAPA, nonconformance, change control ...

next page

Showing results 1-20

All JobsQuality Control Engineer JobsSenior Quality Control Engineer JobsSenior Quality Control Engineer Jobs in Boston, MA

Senior Quality Control Engineer information

See Boston, MA salary details

$65.7K

$114.4K

$159.2K

How much do senior quality control engineer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for senior quality control engineer in Boston, MA is $114,390.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,100.00 and $130,400.00 per year, depending on experience, location, and employer.

What are some common challenges faced by senior quality control engineers in ensuring consistent product quality across multiple production lines?

Senior Quality Control Engineers often encounter challenges such as maintaining uniform quality standards across different production shifts or facilities, managing tight production schedules without compromising on thorough inspections, and adapting to rapid changes in manufacturing processes or technology. To overcome these, they typically implement robust quality management systems, conduct regular training sessions for staff, and utilize data-driven approaches to quickly identify and address variations or defects. Collaboration with cross-functional teams, such as production, R&D, and supply chain, is also crucial to proactively resolve issues and drive continuous improvement.

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

A Senior Quality Control Engineer typically requires a strong background in engineering, quality assurance methodologies, and a bachelor’s degree in a related field, often supplemented by experience in manufacturing or production environments. Familiarity with ISO standards, Six Sigma tools, statistical analysis software, and quality management systems (QMS) is highly valued. Exceptional problem-solving, attention to detail, leadership, and communication skills help drive process improvements and mentor junior staff. These competencies are crucial for ensuring consistent product quality, regulatory compliance, and efficiency within complex production settings.

What does a senior quality control engineer do?

A Senior Quality Control Engineer is responsible for overseeing and improving the quality assurance processes in manufacturing or production environments. They develop and implement testing methods, analyze quality data, and ensure products meet established standards and regulations. Additionally, they often lead teams, train junior staff, and collaborate with other departments to resolve quality issues and drive continuous improvement. Their expertise helps minimize defects, reduce costs, and maintain customer satisfaction.

What is the difference between Senior Quality Control Engineer vs Quality Control Technician?

AspectSenior Quality Control EngineerQuality Control Technician
CredentialsBachelor's degree in engineering or related field, often with certifications like CQEHigh school diploma or associate degree, technical training
Work EnvironmentDesigning quality systems, analyzing data, overseeing testing processesPerforming routine inspections, testing products, recording results
Employer & Industry UsageManufacturing, aerospace, automotive, pharmaceuticalsManufacturing plants, production lines, quality assurance labs
Common Search & ComparisonSenior Quality Control Engineer vs Quality Control Technician

The main difference between a Senior Quality Control Engineer and a Quality Control Technician lies in their responsibilities and qualifications. The engineer typically handles complex analysis, system development, and oversight, requiring higher education and certifications. The technician focuses on routine testing and inspections. Both roles are essential in manufacturing and quality assurance environments, but they differ in scope and expertise.

Senior Quality Control Engineer jobs near you
Infographic showing various Senior Quality Control Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $114,390 per year, or $55 per hour.

Sr. QC Manager

Nova Biomedical

Waltham, MA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 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:
  • Ability to travel between manufacturing facilities as needed.
  • Ability to wear required Personal Protective Equipment (PPE).
  • Ability to stand or sit for extended periods.
  • Ability to work in front of a computer screen for prolonged periods.
  • Ability to lift up to 35 pounds.

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.
Privacy Policy
https://advancedinstruments.showpad.com/share/DmsEd5QTLlqemTYABlvDW

Apply