ZipRecruiter

Log In

1

Quality Control Associate Jobs in Devens, MA (NOW HIRING)

Adecco

QC Inspector

Chelmsford, MA · On-site

$24.20/hr

Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

QC Inspector

Chelmsford, MA · On-site

$24.20/hr

Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Sloan

Quality Control Inspector

Andover, MA · On-site

$54K - $60K/yr

The Quality Control Inspector will be responsible for testing and inspecting components and ... Associate Degree. * Hazardous Waste & USDOT Hazardous Materials. * Power Industrial Truck ...

Kelly Services

Quality Control Inspector

Billerica, MA

$28 - $30/hr

We at Kelly ® hear you, and we're here for you! We're seeking a Manufacturing Technician to work at a premier manufacturing client in Billerica, MA. Pay Rate: $28 to $30 hourly Shift: 1st shift, 7am ...

Sloan

Quality Control Inspector

Andover, MA · On-site

$54K - $60K/yr

The Quality Control Inspector will be responsible for testing and inspecting components and ... Associate Degree. * Hazardous Waste & USDOT Hazardous Materials. * Power Industrial Truck ...

previous pagenext page

Showing results 21-40

All JobsQuality Control Associate JobsQuality Control Associate Jobs in Devens, MA

Quality Control Associate information

See Devens, MA salary details

$12

$28

$42

How much do quality control associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for quality control associate in Devens, MA is $28.33, according to ZipRecruiter salary data. Most workers in this role earn between $20.58 and $34.52 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

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

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

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

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

Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Devens, MA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, 5% Contract, and 2% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $58,933 per year, or $28.3 per hour.

Quality Control Specialist

Kiniksa Pharmaceuticals

Lexington, MA • On-site

$72K - $91K/yr

Full-time

Posted 28 days ago

Job description

Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST®, the first and only FDA-approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders. At Kiniksa, talented individuals are trusted and empowered to make a real impact-shaping the future of medicine while improving the lives of patients who need it most.
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

Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.
Pay Range
$72,000-$91,500 USD
Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.

Apply