Senior GMP QC Analytical Chemist with HPLC/GC

Aequor; Pearl River (NY); On-site; USD 90,000 - 120,000; Full time

Job summary

Aequor is seeking a Quality Control Chemist to join a GMP-regulated QC laboratory environment, focusing on analytical testing for pharmaceutical and biopharmaceutical products. You will document results electronically and support release and stability testing in a compliant, collaborative team setting.

The role requires a Bachelor's or Master’s in a relevant science and at least 5 years in GMP QC labs, with hands-on use of HPLC, GC, and UV and strong GMP documentation practices.

Qualifications

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• Minimum 5 years in a GMP/cGMP QC laboratory environment.
• Experience in pharmaceutical/biopharmaceutical industry required.
• Hands-on with analytical instruments such as HPLC, GC, and UV.
• Strong GMP documentation and regulatory compliance knowledge.
• Experience with electronic laboratory systems and data management tools.

Responsibilities

• Perform laboratory testing of raw materials, drug substances, drugs products, in-process and stability samples.
• Conduct routine wet chemistry and analytical testing using HPLC, GC, CGE, ICE, Osmometer, pH meter, and Conductivity meter.
• Accurately document and review analytical results in LIMS.
• Follow cGMP requirements, SOPs and regulatory guidelines.
• Support audits by maintaining compliant documentation and participate in data peer review.

Skills

Analytical testing

GMP compliance

LIMS data entry

Education

Bachelor’s or Master’s in Chemistry/Biochemistry/Pharmaceutical Sciences

Tools

HPLC

GC

UV

Job description

Aequor is seeking a Quality Control Chemist to join a GMP-regulated QC laboratory environment, focusing on analytical testing for pharmaceutical and biopharmaceutical products. You will document results electronically and support release and stability testing in a compliant, collaborative team setting.

The role requires a Bachelor's or Master’s in a relevant science and at least 5 years in GMP QC labs, with hands-on use of HPLC, GC, and UV and strong GMP documentation practices.