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Fortira Inc

Quality Control Chemist (GMP / Pharmaceutical QC)

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What they do

A Quality Control Chemist uses chemistry analysis to test samples of manufacturing or pharmaceutical products, to ensure that products meet quality standards.

$74,493 / year median in New York

+10% projected growth

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Job Description

Role:
Quality Control Chemist (GMP / Pharmaceutical QC)
Location:
Pearl River, NY -
Onsite Job Summary:
Seeking an experienced Quality Control Chemist with 5+ years of GMP/cGMP pharmaceutical or biopharmaceutical QC laboratory experience. The role involves analytical testing, documentation in LIMS, and ensuring compliance with cGMP standards.
Responsibilities:
  • Perform testing of raw materials, drug substances, drug products, in-process, and stability samples.
  • Operate instruments including HPLC, GC, UV-Vis, pH meter, TOC analyzer, conductivity meter, and related analytical equipment.
  • Document and review results in LIMS.
  • Follow SOPs, cGMP, and regulatory guidelines.
  • Support audits, equipment maintenance, and laboratory documentation.
Requirements:
  • Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  • 5+ years of GMP QC laboratory experience in the pharmaceutical/biopharmaceutical industry.
  • Hands-on experience with HPLC, GC, UV-Vis, and electronic laboratory systems (LIMS).
  • Strong knowledge of cGMP documentation and regulatory compliance.
  • Empower chromatography software experience is a plus.
Work Environment:
  • Laboratory-based role supporting pharmaceutical testing.
  • Requires PPE and adherence to safety procedures for regulated laboratory operations.
Pay:
$38.00 - $42.00 per hour
Work Location:
In person