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
