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Quality Control In Jobs in Warren, RI (NOW HIRING)

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

As a QC Chemist specializing in inhalation products , you'll play a vital role in ensuring the safety, quality, and performance of metered dose inhalers (MDIs) and related dosage forms that patients ...

Cipla

Quality Control (QC) Chemist

Fall River, MA · On-site

$65K - $105K/yr

As a QC Chemist specializing in inhalation products , you'll play a vital role in ensuring the safety, quality, and performance of metered dose inhalers (MDIs) and related dosage forms that patients ...

Whirlpool

Quality Control

Fall River, MA · On-site

$27.05/hr

... with quality control procedures. 27.05 per hour Essential Functions: * Develops, updates, and ... Inspects, tests, and performs audits of components, in-process materials, and finished products for ...

Whirlpool

Quality Control

Fall River, MA · On-site

... with quality control procedures. 27.05 per hour Essential Functions: * Develops, updates, and ... Inspects, tests, and performs audits of components, in-process materials, and finished products for ...

Whirlpool

Quality Control

Fall River, MA

$27.05/hr

In 2025, the company reported approximately $16 billion in annual net sales - close to 90% of which ... Writes and distributes quality control reports and educational material, utilizing internal systems ...

Whirlpool

Quality Control

Fall River, MA · On-site

$27.05/hr

In 2025, the company reported approximately $16 billion in annual net sales - close to 90% of which ... Writes and distributes quality control reports and educational material, utilizing internal systems ...

Amgen, Inc.

Specialist QC

West Greenwich, RI · On-site

In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen. Responsibilities: Analytical Investigation Ownership * Lead Quality Control ...

Amgen

Specialist QC

West Greenwich, RI · On-site

In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen. Responsibilities: Analytical Investigation Ownership * Lead Quality Control ...

Amgen SA

Specialist QC

West Greenwich, RI · On-site

$95 - $125/hr

In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen. Responsibilities: Analytical Investigation Ownership * Lead Quality Control ...

IMPACT TOOL SUPPLY CORP.

Be Seen First

Quality Control Assistant

Woonsocket, RI · On-site

$21 - $26/hr

Looking for experienced Quality Control Assistant ... Must be trained in Geometrical Dimensioning and Tolerancing. This is a part time position that ...

Amgen

Quality Control Associate

West Greenwich, RI · On-site

Associate Quality Control What you will do Let's do this. Let's change the world ... In this vital role you will be responsible for activities including microbiology & analytical ...

Infoway Group

QUALITY CONTROL TECHNICIAN

Mansfield, MA

$19.75 - $25.50/hr

In addition, we are partners with best-in-class technology vendors that enable us to best determine ... Quality Assurance Manufacturing Engineering Research and Development Regulatory Affairs Legal ...

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All JobsQuality Control In JobsQuality Control In Jobs in Warren, RI

Quality Control In information

See Warren, RI salary details

$30.3K

$80.9K

$128.8K

How much do quality control in jobs pay per year?

As of Aug 27, 2026, the average yearly pay for quality control in in Warren, RI is $80,896.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,200.00 and $99,500.00 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 Warren, RI are hiring for Quality Control In jobs?

Cities near Warren, RI with the most Quality Control In job openings:

Quality Control In jobs near you
Infographic showing various Quality Control In job openings in Warren, RI as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $80,896 per year, or $38.9 per hour.

Quality Control (QC) Chemist

Cipla

Fall River, MA • On-site

$65K - $105K/yr

Full-time

Re-posted 6 days ago

Job description

Quality Control (QC) Chemist - Inhalation Products (MDI Focus)

Location: Fall River, MA (On-site)
Schedule: 8:30 AM - 5:00 PM (flex based on production/testing needs)
Salary: $65,000 - $105,000 (based on expertise, especially inhalation experience)

  Bring Precision to Every Breath

Step into a critical role where science meets patient impact. As a QC Chemist specializing in inhalation products, you'll play a vital role in ensuring the safety, quality, and performance of metered dose inhalers (MDIs) and related dosage forms that patients rely on every day.

This is not your average QC role-here, you'll work on complex aerosol and particle-based delivery systems, applying advanced analytical techniques to confirm product integrity and regulatory compliance in a highly controlled cGMP environment.

  What You'll Do

Analytical Testing & Expertise

  • Perform routine and advanced QC testing for pharmaceutical dosage forms, with a strong focus on inhalation products (MDI/DPI systems)
  • Evaluate critical quality attributes (CQA) such as particle size distribution, spray pattern, plume geometry, and dose uniformity
  • Operate and maintain advanced instrumentation:
    • Gas Chromatography (GC)
    • Particle Size Analyzers (e.g., laser diffraction, cascade impaction)
    • ICP (trace elemental analysis)
  • Execute specialized inhalation testing protocols including propellant-based system assessments

Material & Product Understanding

  • Apply working knowledge of raw materials, propellants, excipients, and canister/valve systems specific to aerosol delivery
  • Support testing across multiple dosage forms (solid oral, liquids, injectables, topical, and inhalation platforms)

Data Integrity & Investigations

  • Ensure strict adherence to cGMP, data integrity standards, and ALCOA principles
  • Investigate OOS, deviations, and atypical results, contributing to root cause analysis and corrective actions

Documentation & Compliance

  • Maintain accurate, audit-ready documentation aligned with FDA and regulatory expectations
  • Follow and continuously improve SOPs in a structured QC environment
  What Makes You a Strong Candidate

Education & Technical Background

  • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or Physics (highly preferred fields aligned with role expectations)
  • Strong foundation in analytical techniques and data interpretation

Industry Experience

  • Proven experience in a pharmaceutical QC environment (required)
  • Hands-on exposure to multiple dosage forms, especially:
    • Tablets/Capsules
    • Liquid formulations
    • Injectables
    • Topicals
    • MDI/DPI inhalation products (highly preferred)

Functional Expertise

  • Experience specifically in Quality Control roles (primary function)
  • Comfortable working in a fully onsite, regulated lab environment with fixed schedules and SOP-driven workflows
  • Strong communication skills and ability to interpret, document, and present scientific findings
  Work Environment
  • Operate in a state-of-the-art cGMP laboratory handling solvents, powders, and aerosol systems
  • Required use of PPE: lab coats, safety glasses, respirators, etc.
  • May include shift flexibility (day/evening/night) and occasional weekends based on production demands
  Physical Requirements
  • Stand/walk for extended periods (~75% of shift)
  • Lift up to 10 kg as needed
  • Perform detailed lab work requiring precision and focus
  Why This Role Stands Out

Inhalation Expertise - Work on advanced drug delivery systems that directly impact respiratory health
Technical Depth - Go beyond routine testing into specialized aerosol science and complex analytics
Career Growth - Build niche expertise in a high-demand domain within pharmaceuticals
Quality at the Core - Be a trusted gatekeeper ensuring every product meets the highest standards

  Important Notes
  • This is a fully onsite role (no remote or hybrid options)
  • Candidates must be authorized to work in the U.S. (no sponsorship available)

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.


  About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.  

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