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Quality Control Associate Jobs in Tiverton, RI (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 ...

Cipla

QC Sampling Associate

Fall River, MA

$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 ...

JSI Cabinetry

Warehouse Inventory Control

Fall River, MA · On-site

$17.50 - $21.50/hr

... of the highest quality cabinetry. JSI operates distribution facilities in Fall River, Chicago ... JSI Cabinetry is seeking a motivated and detail-oriented entry level Inventory Control Associate to ...

Careers | CET

Quality Associate

Bristol, RI

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

Cresco Labs

Inventory Control Agent

Fall River, MA

$17 - $21/hr

Our portfolio of in-house cultivated and manufactured brands features some of the highest quality ... We are looking for associates with great attention to detail to maintain an accurate inventory. The ...

Cresco Labs

Inventory Control Agent

Fall River, MA · On-site

$17 - $21/hr

Our portfolio of in-house cultivated and manufactured brands features some of the highest quality ... We are looking for associates with great attention to detail to maintain an accurate inventory. The ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Tiverton, RI

Quality Control Associate information

See Tiverton, RI salary details

$11

$25

$37

How much do quality control associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for quality control associate in Tiverton, RI is $25.05, according to ZipRecruiter salary data. Most workers in this role earn between $18.22 and $30.53 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 Tiverton, RI are hiring for Quality Control Associate jobs? Cities near Tiverton, RI with the most Quality Control Associate job openings:
Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Tiverton, RI as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $52,108 per year, or $25.1 per hour.

QC Sampling Associate

Cipla

Fall River, MA • On-site

$25 - $29/hr

Full-time, Other

Posted 24 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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