Quality Control Associate

Meet Life Sciences Ltd.; Morrisville (NC); On-site; USD 52,000 - 75,000; Full time

Job summary

Meet Life Sciences Ltd. is seeking a QC Associate to perform analytical testing in a cGMP pharmaceutical manufacturing setting, ensuring materials, in-process samples, and finished products meet quality standards.

The role involves using HPLC, GC, FTIR, and moisture analysis, preparing samples and reagents, and documenting results in compliance with SOPs. OOS investigations and audits may be involved.

Qualifications

• Associate’s or Bachelor’s degree in Chemistry, Biology, or related field.
• Experience in a QC laboratory in GMP environment preferred.
• Familiarity with HPLC, GC, FTIR is advantageous.

Responsibilities

• Perform routine analytical testing using HPLC, GC, FTIR, and moisture analysis.
• Prepare samples, reagents, and standards for testing.
• Review and document laboratory results per cGMP and SOPs.
• Maintain accurate lab records and data integrity.
• Support method development, validation, and troubleshooting.
• Investigate OOS results and laboratory deviations.
• Maintain equipment, supplies, and a compliant work environment.
• Support product release testing, audits, and inspections.

Skills

Analytical testing

Lab compliance

Data integrity

OOS investigation

Education

Associate’s or Bachelor’s degree in Chemistry/Biology or related field

Tools

HPLC

GC

FTIR

Moisture analysis

Job description

The QC Associate performs analytical testing and supports quality control activities within a cGMP-regulated pharmaceutical manufacturing environment, ensuring raw materials, in-process samples, and finished products meet established quality standards.

Responsibilities

• Perform routine analytical testing using laboratory techniques such as HPLC, GC, FTIR, and moisture analysis.
• Prepare samples, reagents, and standards for testing.
• Review and document laboratory results in compliance with cGMP requirements and SOPs.
• Maintain accurate laboratory records and ensure data integrity.
• Support analytical method development, validation, and troubleshooting as needed.
• Investigate out-of-specification (OOS) results and laboratory deviations.
• Maintain laboratory equipment, supplies, and a clean, compliant work environment.
• Support product release testing, audits, and regulatory inspections.

Qualifications

• Associate’s or Bachelor’s degree in Chemistry, Biology, or a related scientific field.
• Experience in a QC laboratory within pharmaceutical manufacturing or another GMP-regulated environment preferred.
• Familiarity with analytical instrumentation, including HPLC, GC, and FTIR, is an advantage.
• Knowledge of cGMP regulations, SOPs, laboratory documentation, and data integrity.