QC Chemist II – Analytical Testing & Method Transfer

Staffing Resource Group, Inc; Largo (FL); On-site; USD 39,000 - 45,000; Part time

Job summary

SRG4 Life Sciences in Largo, FL is seeking a QC Chemist II to perform analytical testing and method transfer in a GMP-regulated contract environment. You will apply HPLC, GC, ICP, AA, and other techniques to support pharmaceutical manufacturing and quality control.

The role emphasizes documentation, compliance with cGMP and GLP, and collaboration with QA and validation teams on testing, investigations, and CAPAs. This is a contract, 2nd shift position offering competitive pay.

Qualifications

• Bachelor's degree in Chemistry or related discipline.
• Two+ years in an analytical laboratory in FDA-regulated industry.
• Experience with HPLC, GC, ICP and related testing assays.
• Knowledge of compendia testing and FDA regulations.
• Ability to use a PC for data entry and reporting.

Responsibilities

• Transfer and testing of analytical methods.
• Revise Test Methods and SOPs.
• Test incoming materials using compendial methods (USP/PhEUR/JP).
• Test stability, in-process, and finished product samples with multiple techniques.
• Record raw data, analyze results, and interpret data.
• Investigate OOS, implement CAPAs and corrective actions.
• Ensure GLP, cGMP, cUSP and SOP compliance.
• Maintain reagents, MSDS, and PPE; support validation activities.
• Promote GMP and safety; assist with troubleshooting and QA interactions.
• Contribute to continuous improvement and problem solving.

Skills

Analytical testing

cGMP knowledge

FDA regulations knowledge

Documentation & data recording

Problem solving

Communication skills

Education

Bachelor's degree in Chemistry or related discipline

Tools

HPLC

GC

ICP

UV/VIS

Infrared spectroscopy

Atomic absorption

pH/Viscosity/Specific gravity

Job description

SRG4 Life Sciences in Largo, FL is seeking a QC Chemist II to perform analytical testing and method transfer in a GMP-regulated contract environment. You will apply HPLC, GC, ICP, AA, and other techniques to support pharmaceutical manufacturing and quality control.

The role emphasizes documentation, compliance with cGMP and GLP, and collaboration with QA and validation teams on testing, investigations, and CAPAs. This is a contract, 2nd shift position offering competitive pay.