Quality Control Analyst

Quality Control Analyst

Laboratory

Huntington, WV, US

Pay Rate Low: 30 | Pay Rate High: 35

Our client is a well-established company in the healthcare and pharmaceutical manufacturing industry is seeking a Quality Control Analyst to join its laboratory operations team in Huntington, WV. This role focuses on performing a wide range of routine and non-routine analytical testing to ensure product quality and compliance with regulatory standards.

Located in Huntington, WV

6 month contract with extension

Pay: $30-35/hour

1st shift schedule

Key Responsibilities:

Conduct quantitative analyses using GC, HPLC, and GC-Headspace, including calibration standard preparation

Execute qualitative testing such as UV-Vis, IR identification, reagent-based ID tests, pH, conductivity, turbidity, TLC for impurities, refractive index, melting point/flow, and cytotoxicity testing

Perform moisture and raw material testing, including sampling

Carry out special and routine testing based on laboratory needs

Review analytical lab data for accuracy and compliance

Support laboratory investigations including OOS (Out of Specification), NCI (Non-Conformance Investigation), DCT (Deviation Control Tracking), and CAPA (Corrective and Preventive Actions)

Participate in analytical method improvement, validation, and transfer efforts

Perform equipment maintenance, calibration, and troubleshooting

Assist in the execution of protocols for validation and qualification processes

Prepare laboratory solutions and mobile phases for HPLC

Maintain a clean and organized laboratory, including cleaning of glassware and equipment depyrogenation

Manage inventory of lab materials and support supply purchasing

Ensure proper documentation, archiving, and flow of lab records

Provide technical training and support for lab associates as needed

Qualifications:

Bachelor's degree in Chemistry, Biochemistry, or a related scientific field

1-3 years of experience in a laboratory or pharmaceutical manufacturing environment preferred

Experience with analytical instrumentation (HPLC, GC, UV-Vis, etc.)

Strong attention to detail and excellent documentation practices

Familiarity with cGMP, GLP, and FDA regulations is a plus

**This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!**

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