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

AMRI

QC Microbiologist II

Hopkinton, MA

$74K - $85K/yr

Receive QC microbiological sample for internal testing, login, processing, tracking, distribution of test results, and closure * Assist QC management to author, review and approve documentation ...

Curia, Inc.

QC Microbiologist II

Hopkinton, MA · On-site

$74K - $85K/yr

Receive QC microbiological sample for internal testing, login, processing, tracking, distribution of test results, and closure * Assist QC management to author, review and approve documentation ...

Amrize

Quality Control Technician II

Saugus, MA · On-site

$19 - $24.50/hr

Assists manager with customer service issues as directed. Certifies results of laboratory findings. Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH

Cox Engineering

Quality Assurance Manager

Randolph, MA · On-site

$100K - $120K/yr

Job Title: QA/QC Manager Position Summary The QA/QC Manager leads the Quality function at the Cambridgeport manufacturing plant, with full accountability for product quality across custom HVAC and ...

Amrize

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Assists manager with customer service issues as directed. Certifies results of laboratory findings. Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH

Amrize

Quality Control Technician II

Saugus, MA · On-site

$19 - $24.50/hr

Assists manager with customer service issues as directed. Certifies results of laboratory findings. Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH

Amrize

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Assists manager with customer service issues as directed. Certifies results of laboratory findings. Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH

Dyne Tx

Director, Quality Control

Waltham, MA · On-site

$190 - $230/hr

... Management to align quality and program objectives * Oversees stability and reference standard ... and/or Quality Control within a GMP‑regulated environment Strong expertise in analytical ...

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Quality Control Manager information

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How much do quality control manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for quality control manager in Canton, MA is $85,992.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $105,700.00 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 Canton, MA? The most popular types of Quality Control jobs in Canton, MA are:
What job categories do people searching Quality Control Manager jobs in Canton, MA look for? The top searched job categories for Quality Control Manager jobs in Canton, MA are:
What cities near Canton, MA are hiring for Quality Control Manager jobs? Cities near Canton, MA with the most Quality Control Manager job openings:
Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Canton, MA as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $85,992 per year, or $41.3 per hour.

Director, Quality Control

Sebela Pharmaceuticals Inc.

Holbrook, MA • On-site

Full-time

Re-posted 2 days ago

Job description

Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in Gastroenterology and a focus on innovation in Women’s Health. Our Vision is to build the leading Gastroenterology company in the U.S., with a complementary
focus on innovation in Women’s Health, premised on our expertise in pharmaceutical development and commercialization. Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and manufacturing organization (CDMO) in Holbrook, MA, offering pharmaceutical-development and in-house manufacturing services for specialty gastroenterology products.
We value dedication, energy, and enthusiasm, and we focus on innovation and results while striving to achieve our corporate mission and vision. Sebela Pharmaceuticals is committed to cultivating an inclusive environment where all employees are treated with respect. We accomplish this by fostering a culture of diversity, equity and inclusion, which is essential to innovation and continuous improvement. Sebela operates from three locations in Roswell, Georgia, Braintree and Holbrook, MA and headquarters in Dublin, Ireland.
This position is responsible for leading Quality Controls Laboratory operations at the Holbrook site including the development, implementation and maintenance of quality control systems and activities to support commercial manufacturing and new product introductions.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
  • Provide strategic leadership and oversight of QC operations, ensuring alignment with company objectives for product quality, regulatory compliance, and business performance.
  • Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.
  • Review and approve QC specifications, procedures, protocols, validation documents, and analytical methods related to raw materials, intermediates, and commercial products.
  • Ensure all testing is performed in accordance with internal procedures and cGMP requirements.
  • Lead investigations into Out-of-Specification (OOS) results and laboratory deviations ensuring timely root cause identification and implementation of effective corrective and preventive actions (CAPAs).
  • Maintain inspection readiness across QC operations, supporting regulatory inspections, customer audits, and internal quality audits.
  • Oversee laboratory change control processes, risk assessments, equipment qualification activities, and implementation of compliant operational improvements.
  • Ensure critical laboratory equipment is appropriately qualified, calibrated, maintained, and operated to support reliable testing and maintain data integrity.
  • Ensure laboratory data integrity, documentation accuracy, and adherence to ALCOA principles
  • Partner with Quality Assurance, Manufacturing, and external stakeholders to investigate product quality issues and drive continuous improvement initiatives.
  • Lead supplier quality support activities, including supplier qualification, performance monitoring, and resolution of supplier-related quality issues.
  • Monitor and analyze QC performance metrics and quality system trends to identify risks, drive operational excellence, and strengthen compliance.
  • Develop, mentor, and retain a high-performing QC organization, fostering a culture of accountability, collaboration, and continuous professional development.
  • Manage departmental budgets, capital planning, and resource requirements to ensure effective execution of business and quality objectives.
  • Other duties as assigned.
KEY COMPETENCIES:
  • Leadership and teamwork
  • Regulatory Compliance, cGMP, Statistical Process Control
  • Extensive analytical chemistry experience
  • Project management
  • Data collection, management and analysis
  • Ability to direct and be resilient and focused under pressure
  • Planning and time management
  • Strong decision-making skills
  • Ability to manage multiple priorities
  • Ability to foster excellent working relationships across all levels, internal/external customers and suppliers
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential function satisfactorily, be flexible in terms of work hours, and have strong knowledge and experience in cGMPs and Oral Dose Pharmaceutical Production Processes. The requirements listed below are representative of the knowledge, skills and/or abilities required.
  • BS or master’s degree in chemistry, biology, or other pharmaceutical science related field.
  • Minimum of 8-10 years QC management experience working in pharmaceutical finished product manufacturing with experience in compliance, quality control, and regulatory development.
  • Direct experience interacting with FDA and other regulatory agencies.
  • Strong knowledge and understanding of FDA cGMP regulations.
  • Experienced in GMP audits, including drug product manufacturing and analytical testing sites.
  • Ability to build collaborative relationships and lead effectively in a cross-functional environment.
  • Self-motivated and results-driven leader with a proactive, hands-on approach.
  • Strong organizational, prioritization, and time management skills, coupled with strong critical-thinking abilities to evaluate complex challenges, solve problems effectively, and drive continuous improvement.
  • Strong project management skills.
  • Excellent written and oral communication / presentation skills.
  • Adept at and comfortable with statistical analysis.
Pay Range: $150-190K base (this reflects our reasonable and good faith estimate of what will be paid at the time of posting). Competitive benefits package included.

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