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Quality Associate Jobs in Massachusetts (NOW HIRING)

Cipla

QC Sampling Associate

Fall River, MA · On-site

$25 - $29/hr

Job Title: QC Sampling Associate FLSA Classification : Full-Time, Non-Exempt/Hourly Professional Work Location: Fall River, MA Work Hours : General Shift: 8:300 AM - 5:00 PM (may vary based on ...

Integrated Resources INC

QA Associate

Billerica, MA · On-site

The Quality Assurance Specialist will work directly with validation project coordinators, technical area representatives and laboratory management Primary responsibilities are reviewing laboratory ...

Textron

Assoc Quality Inspector

Wilmington, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

Textron

Assoc Quality Inspector

Wilmington, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

Textron

Assoc Quality Inspector

Wilmington, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

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All JobsQuality Associate JobsQuality Associate Jobs in Massachusetts

Quality Associate information

See Massachusetts salary details

$12

$29

$55

How much do quality associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality associate in Massachusetts is $29.41, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $34.38 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

What are the key skills and qualifications needed to thrive as a quality associate, and why are they important?

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

More about Quality Associate jobs

What are the most commonly searched types of Quality jobs in Massachusetts?

The most popular types of Quality jobs in Massachusetts are:

What are popular job titles related to Quality Associate jobs in Massachusetts?

For Quality Associate jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Quality Associate jobs in Massachusetts look for?

The top searched job categories for Quality Associate jobs in Massachusetts are:

What cities in Massachusetts are hiring for Quality Associate jobs?

Cities in Massachusetts with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $61,179 per year, or $29.4 per hour.

QC Sampling Associate

Cipla

Fall River, MA • On-site

$25 - $29/hr

Full-time, Other

Posted 27 days ago

Job description

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.
Job Title: QC Sampling Associate
FLSA Classification: Full-Time, Non-Exempt/Hourly Professional
Work Location: Fall River, MA
Work Hours: General Shift: 8:300 AM - 5:00 PM (may vary based on business needs)
Reports To: Quality Control Manager
Hourly Rate: $25 - $29
Duties and Responsibilities:
The general duties and responsibilities of the Quality Control Lab Technician include but are not limited to the following:
  • Perform sample withdrawal for all incoming raw materials, packing materials, water including but not limited to receipt, logging distribution and destruction.
  • Update all sample information in SAP as per company procedures.
  • Complete data entry as required.
  • Oversee temperature and humidity monitoring for retention and sample storage rooms.
  • Conduct sample loading in stability chambers and submitting stability samples as per schedule.
  • Provide general housekeeping in the QC lab and any other functional activity as assigned by management.
  • Maintaining and updating the retention rooms of raw materials as required.
  • Cleaning of sampling area and sampling accessories as per approved SOPs.
  • Ensure all sampling activities comply with cGMP, data integrity, and safety requirements.
  • Follow contamination-control practices during sampling, including gowning and cleanroom behavior when applicable.
  • Accurately label, log, and submit samples to the QC laboratory with complete documentation.
  • Maintain and verify cleanliness and readiness of sampling tools and equipment.
  • Support material status control by ensuring sampled materials are properly segregated and labeled.
  • Document sampling activities in logbooks, sampling records, and electronic systems (SAP/ILMS) in a timely and accurate manner.
  • Assist in investigations related to deviations, out-of-specification (OOS) results, or sampling errors, as required.
  • To participate in GDP, cGMP, and safety training programs.
  • Maintain compliance with site safety policies and participate in EHS initiatives.
  • Support audit and inspection readiness by ensuring sampling documentation is complete and inspection-ready at all times.
  • Coordinate and dispatch samples to contract testing laboratories (CTLs) or other InvaGen/Cipla laboratories as per approved procedures and testing requirements.
  • Maintain stock of sampling equipment and consumables.
  • Other duties as assigned.

Education and Experience:
  • Minimum of High School Diploma or equivalent education credential (ex. GED) required.
  • Proficient user of Microsoft Office Programs to include Word, Excel, Outlook, PowerPoint, and other lab-related systems.
  • 2 years' work experience in a pharmaceutical, raw materials sampling activity.
  • Associates degree or higher in Chemistry, Laboratory Science, or related fields of study from an accredited institution. (Preferred)
  • Proficiently speak English as a first or second language
  • Have excellent organization, learning and teaching skills required to work in teams
  • Ability to understand and analyze complex data.
  • Working knowledge of Microsoft Office programs and other scientific based software.
  • Experience in pharmaceuticals is a plus.

Professional and Behavioral Competencies
  • Hourly position.
  • Full time
  • Must be willing to work in a pharmaceutical packaging setting.
  • Must be willing and able to work any assigned shift ranging from first or second shift.
  • Work schedule may be Monday to Friday.
  • Must be willing to work some weekends based on business needs as required by management.
  • Must possess a positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors.
  • No remote work available
  • No employment sponsorship or work visas.

Working conditions
This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Long periods of standing up/walking during working hours; ability to ascent/decent ladders; and able to lift to 35 pounds.
GLOBAL COMPANY
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
EEO Statement
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

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