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Quality Control In Jobs in Peabody, MA (NOW HIRING)

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

S. manufacturing facilities in Waltham, Norwood, and Billerica, Massachusetts, supporting the ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

PGI Foods

Quality Control Technician

Lowell, MA

$20 - $24/hr

Quality Control Technician Lowell, MA $20-$24/hour, depending on experience Full-Time | Monday ... In this hands-on position, you'll perform product testing, monitor production processes, and help ...

PGI Foods

Quality Control Technician

Lowell, MA

$20 - $24/hr

Quality Control Technician ???? Lowell, MA ???? $20-$24/hour, depending on experience ... In this hands-on position, you'll perform product testing, monitor production processes, and help ...

PGI Foods

Quality Control Technician

Lowell, MA

$20 - $24/hr

Quality Control Technician Lowell, MA $20-$24/hour, depending on experience Full-Time | Monday ... In this hands-on position, you'll perform product testing, monitor production processes, and help ...

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Showing results 1-20

All JobsQuality Control In JobsQuality Control In Jobs in Peabody, MA

Quality Control In information

See Peabody, MA salary details

$33.9K

$90.3K

$143.7K

How much do quality control in jobs pay per year?

As of Aug 30, 2026, the average yearly pay for quality control in in Peabody, MA is $90,269.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,200.00 and $111,000.00 per year, depending on experience, location, and employer.

What is the difference between Quality Control In vs Quality Control Inspector?

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What does a quality control in job do?

A quality control in job involves inspecting products or services to ensure they meet specified standards and quality requirements. It includes tasks such as testing, measuring, and reviewing processes, often using tools like checklists or testing equipment, to identify defects and ensure customer satisfaction.

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

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

Quality Control In jobs near you
Infographic showing various Quality Control In job openings in Peabody, MA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $90,269 per year, or $43.4 per hour.

Quality Control Specialist

Kiniksa Pharmaceuticals

Lexington, MA • On-site

Full-time

Posted 25 days ago

Job description

Reporting to the Associate Director, Quality Control - Stability and Trending, the Stability Coordinator manages the GMP stability programs, supporting trending of methods, reference standard, and stability data to improve process and product understanding, and to support problem solving and decision making.  The successful candidate will support clients across Kiniksa, including Analytical Development, Quality Control, Manufacturing, CMC, Validation, and Quality Systems. 

This role is based in our Lexington, MA office and requires employees to be onsite five days per week.

Responsibilities (including, but not limited to):

  • Oversee systems supporting GMP stability programs including tracking and trending of stability data, generation of protocols and reports, and driving timely completion of quality records
  • Maintain stability testing records and results within the stability software to assure traceability and availability of records
  • Collaborate with contract laboratories to ensure timely completion of testing and delivery of QC deliverables for stability programs
  • Review and approve laboratory data and results, ensuring their traceability and integrity
  • Generate and present stability metrics to support annual reports, regulatory filings, and internal decision-making
  • Perform routine trending of stability data to support shelf-life of GMP products
  • Evaluate product stability data to establish and extend product shelf-life
  • Coordinate shipping and sample management of routine and non-routine testing activities
  • Drive process improvements and ensure inspection readiness (ISO, GMP alignment) for area of responsibility
  • Create and improve procedures related to GMP stability programs
  • Support batch certificate and Certificates of Analyses generation and additional tasks as required
  • Participate in the authoring and review of QC protocols and stability reports

Standout Skills for Impact:

  • Proven ability to manage projects and work with cross-functional teams comprised of internal and/or external contacts, including CTLs
  • Proactive, with a strong desire to engage with clients, and act with urgency and passion
  • Strong ownership mindset with the ability to drive timelines and resolve issues in collaboration with internal teams and external partners
  • Ability to translate stability data and trends into clear insights that support decision-making, regulatory strategy, and product lifecycle management

Qualifications and Experience:

  • BS in a scientific area with 3-5 years of experience in Quality Control in a GMP setting
  • Working knowledge of statistical tools, methodologies, and related software, including experience with JMP as a plus
  • Experience working with contract testing laboratories or external vendors in a regulated environment
  • Ability to review analytical data for completeness, accuracy, traceability, and compliance with applicable procedures
  • Effective verbal and written communication skills
  • Proven ability to work with a high level of integrity, accuracy, and attention to detail
  • Familiarity with ICH stability guidelines and expectations for pharmaceutical products
  • Knowledge of quality systems and domestic and international regulatory requirements
 

Apply