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Quality Control; QC Chemist

Job in Fall River, Bristol County, Massachusetts, 02722, USA
Listing for: CIPLA LTD
Full Time, Per diem position
Listed on 2026-05-24
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 65000 - 105000 USD Yearly USD 65000.00 105000.00 YEAR
Job Description & How to Apply Below
Position: Quality Control (QC) Chemist
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 Inva Gen Pharmaceuticals, a Cipla subsidiary Inva Gen Pharmaceuticals, Inc. is engaged in the development,…
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