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

Maintain the QA Document Control Records room and associated archive locations as per applicable ... Associate or bachelor's degree preferred. * Excellent written and verbal communication skills.

Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...

Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...

Quality Control Technician II

Saugus, MA · On-site

$19 - $24.50/hr

Quality Control Technician II | Req ID: 16555 | HR Contact: Roscoe Chambers | Location: Saugus ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Quality Control Technician II

Saugus, MA · On-site

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Showing results 21-40

Quality Control Associate information

See Quincy, MA salary details

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How much do quality control associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for quality control associate in Quincy, MA is $26.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.47 and $32.60 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 are the most commonly searched types of Quality Control jobs in Quincy, MA? The most popular types of Quality Control jobs in Quincy, MA are:
What are popular job titles related to Quality Control Associate jobs in Quincy, MA? For Quality Control Associate jobs in Quincy, MA, the most frequently searched job titles are:
What cities near Quincy, MA are hiring for Quality Control Associate jobs? Cities near Quincy, MA with the most Quality Control Associate job openings:
Infographic showing various Quality Control Associate job openings in Quincy, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $55,688 per year, or $26.8 per hour.

QC Raw Material Scientific Sr. Associate/Associate (Contract) 29688

Vertex Pharmaceuticals

Boston, MA

$42 - $48/hr

Full-time

Posted 15 days ago


Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

78th of 86 rated pharmaceutical


Job description

The QC raw material scientific/sr. scientific associate operates independently to perform raw material testing such as appearance and ID of materials including but not limited to small molecules, chemicals, solvents and gases. The associate will be responsible for supporting shipment of samples to external contract testing labs which includes - process and receipt in LIMS, packaging of samples at appropriate storage conditions, completion of respective vendor sample submission form, and processing of final results in LIMS/associated internal forms. The associate will also be responsible for performing particle characterization of foreign particulates found in various sample types (i.e. finished product, cryopreserved intermediate, water flushing). The ideal candidate will have expertise in particle analysis techniques and instrumentation as well as conducting various raw material analytical testing.

** The identified candidate will need to pass a vision and color blindness test **

Key Duties and Responsibilities:

  • Works with multiple functional groups to meet business needs.
  • Performs internal raw material testing per associated material specification to support GMP operations
  • Supports shipment of samples to external contract testing labs for respective testing per associated material specification
  • Characterize sub-visible and visible particulates by FTIR and optical microscopy
  • Individual should be capable of writing reports related to work completed in laboratory.
  • Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines. 
  • Problem solving, either independently or with assistance pertaining to extraction of particulates and/or instrumentation problems. 
  • Performs work assignments accurately, and in a timely and safe manner
  • Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP)
  • Performs self and peer review of the data for accuracy and compliance

Knowledge and Skills:

  • Team focused, demonstrate high level of integrity, and have strong collaboration, communication, interpersonal and organizational skills
  • Prior experience using FTIR and raw material testing experience
  • Knowledge of multiple applicable techniques such as: particle size, microscopy
  • Proficient in Microsoft Excel and Word 
  • Proven ability in technical writing skills 
  • Proven problem solving and troubleshooting abilities 
  • Good written and oral communication skills 
  • Ability to work in a collaborative work environment with a team
  • Experience being involved with analytical investigations/deviations 

Education and Experience:

  • Bachelor’s degree in a biologic field, life sciences, engineering, chemistry, pharmaceutical science.
  • At least 5 years’ experience in the pharmaceutical industry, biotech industry, life sciences industry.
  • Particle ID and raw material experience is a plus

Work Hours

  • Standard Hours: Monday – Friday 8:00am - 4:30pm (with flexibility to support second shift / weekends as needed)

$35-42/hr (Associate) $42-48/hr (Sr. Associate)


This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice.   Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners

(collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.

If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors

 

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