Pharma QC Chemist - HPLC/cGMP Expert (NJ)

Garonit Pharma; Northern (KY); Hybrid; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) with Company match

PTO and paid holidays

Job summary

Garonit Pharmaceutical seeks a Quality Control Chemist to join our Quality team at our Flanders, NJ facility. The role supports analytical testing and laboratory operations to ensure compliance with cGMP and regulatory requirements.

The ideal candidate will have a Bachelor's degree in Chemistry or Life Sciences and 3–5+ years in a regulated QC lab, with experience in HPLC and USP methods, ensuring detailed documentation and adherence to SOPs.

Qualifications

• Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline.
• 3–5+ years of experience in a Quality Control laboratory.
• Experience with pharmaceutical analytical testing and cGMP requirements.
• Experience operating HPLC and other analytical laboratory instrumentation.

Responsibilities

• Perform sampling and analytical testing of raw materials, in-process materials, finished products, and packaging components.
• Operate, maintain, and troubleshoot laboratory instrumentation, including HPLC and other analytical equipment.
• Support laboratory investigations, deviations, OOS results, and CAPA activities.
• Assist with analytical method development, transfer, verification, and validation activities.
• Maintain accurate and complete laboratory documentation per cGMP requirements and Company procedures.

Skills

Quality Control

Regulatory compliance

Documentation

Education

Bachelor’s degree in Chemistry/Life Sciences

Tools

HPLC

Analytical instrumentation

Job description

Garonit Pharmaceutical seeks a Quality Control Chemist to join our Quality team at our Flanders, NJ facility. The role supports analytical testing and laboratory operations to ensure compliance with cGMP and regulatory requirements.

The ideal candidate will have a Bachelor's degree in Chemistry or Life Sciences and 3–5+ years in a regulated QC lab, with experience in HPLC and USP methods, ensuring detailed documentation and adherence to SOPs.