Quality Control Analyst

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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