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

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

Onsite in Fall River, MA

Schedule: 8:30 AM – 5:00 PM (flex based on production/testing needs)

Full-Time

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

Job Type: Full-Time, Permanent