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Quality Control Jobs in Randolph, MA (NOW HIRING)

Tech Etch

Quality Control Inspector

Plymouth, MA · On-site

$17.50 - $25/hr

ABOUT THE JOB The Quality Control Inspector conducts in-process inspection sampling of manufactured parts, incoming inspection on parts and supplies used for the manufacture of products, First ...

System One

QC Technician

Canton, MA · On-site

$25/hr

Job Title: QC Technician Location: Canton, MA Type: Contract To Hire Compensation: $25 Work Model: Onsite - onsite Hours: 1st Shift M-F Responsibilities * Perform daily quality tests and inspections ...

Sebela Pharma

QC Chemist

Holbrook, MA · On-site

$55K - $60K/yr

The QC Chemist is a laboratory bench position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. PRINCIPAL DUTIES AND ...

Plansee Group

Quality Control Inspector

Franklin, MA · On-site

$25 - $29/hr

Accurately completes all quality control documentation such as non-conforming material, travelers and control charts. * Create and store electronic inspection reports using customer drawings and ...

Tech Etch

Quality Control Inspector

Plymouth, MA

$17.50 - $25/hr

ABOUT THE JOB The Quality Control Inspector conducts in-process inspection sampling of manufactured parts, incoming inspection on parts and supplies used for the manufacture of products, First ...

Replimune-2

Scientist I, Quality Control

Framingham, MA · On-site

$112.50 - $146/hr

The Scientist I/II, QC Analytical will perform QC testing according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role may also include the ...

Replimune

Scientist I, Quality Control

Framingham, MA · On-site

$112K - $146K/yr

The Scientist I/II, QC Analytical will perform QC testing according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role may also include the ...

Lexington Medical, Inc.

Quality Control Technician

Bedford, MA · On-site

$19.75 - $25.25/hr

As a Quality Control Technician at Lexington Medical, you will be responsible for inspecting medical device components and finished products to ensure they meet our rigorous quality standards. You ...

Replimune

Scientist II, Quality Control

Framingham, MA · On-site

$124K - $165K/yr

The Scientist II, QC Analytical will perform QC testing according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role may also include the ...

New

Nova Biomedical Corporation

Sr. QC Manager

Waltham, MA · On-site

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 ...

Nova Biomedical

Sr. QC Manager

Waltham, MA · On-site

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 ...

Nova Biomedical

Sr. QC Manager

Waltham, MA

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 ...

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Quality Control information

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How much do quality control jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for quality control in Randolph, MA is $21.90, according to ZipRecruiter salary data. Most workers in this role earn between $17.64 and $24.52 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.
More about Quality Control jobs

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

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

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

Quality Control jobs near you
Infographic showing various Quality Control job openings in Randolph, MA as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 22% Part Time, 3% Temporary, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $45,547 per year, or $21.9 per hour.

QC Chemist

Sebela Pharmaceuticals Inc.

Holbrook, MA

$55/hr

Full-time

Re-posted 7 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.
The QC Chemist is a laboratory bench position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment.
PRINCIPAL DUTIES AND RESPONSIBILITIES
  • Perform testing of raw materials, in-process materials, and finished products according to approved laboratory test methods
  • Perform instrument qualification and maintenance
  • Perform test method validation/verification
  • Review analytical data for completeness, accuracy, and compliance
  • Perform training on procedures, equipment, or quality systems
  • Revise SOPs, Worksheets, and Forms as needed
  • Individual contributor role, but may be assigned as a project lead or trainer commensurate with experience or expertise
  • Other duties as assigned
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential function satisfactorily, be flexible in terms of work hours, have strong knowledge and experience in analytical scientific skills, and a strong attention to detail. The requirements listed below are representative of the knowledge, skills and/or abilities required.
  • Minimum bachelor’s degree in chemistry, or related discipline
  • 0-2 years of experience in a cGMP environment, preferably in a laboratory setting
  • Strong foundation in analytical techniques and data interpretation
  • Excellent attention to detail and ability to follow detailed procedures which contribute to QC laboratory readiness and compliance
Pay Range: $55-60K based on experience (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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