More jobs:
Quality Control; QC Chemist
Job in
Fall River, Bristol County, Massachusetts, 02722, USA
Listed on 2026-05-24
Listing for:
CIPLA LTD
Full Time, Per diem
position Listed on 2026-05-24
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst
Job Description & How to Apply Below
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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