Cipla

Quality Control (QC) Chemist

Cipla$65K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or Physics is preferred
  • Proven experience in a pharmaceutical QC environment
  • Hands-on exposure to multiple dosage forms, with a preference for inhalation products
  • Experience in Quality Control roles, with a focus on analytical techniques
  • Strong communication skills for interpreting, documenting, and presenting scientific findings

Responsibilities

  • Perform routine and advanced QC testing for inhalation products focusing on MDI/DPI systems
  • Evaluate critical quality attributes such as particle size distribution and dose uniformity
  • Operate and maintain advanced instrumentation like Gas Chromatography and Particle Size Analyzers
  • Execute specialized inhalation testing protocols for propellant-based systems
  • Contribute to investigations of OOS and atypical results, aiding in root cause analysis
  • Maintain accurate and compliant documentation aligned with FDA expectations
  • Continuously improve SOPs in a structured QC environment

Benefits

  • Opportunity to work in a state-of-the-art cGMP laboratory
  • Gain experience in complex aerosol science and specialized analytical techniques
  • Possibility for ongoing career growth in a high-demand pharmaceutical domain
  • Be part of a team that prioritizes quality and patient safety
Full 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)


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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