Job Description

Job Title: QC Analyst - Pharma (Only W2, No C2C)

Location: Greenville, NC

Duration: Long-Term Contract (12+ Months, potential for extension)

Industry : Core Pharma

Key Responsibilities:

• Perform analytical testing of pharmaceutical samples (raw materials, intermediates, and finished products) in compliance with SOPs and cGMP regulations.
• Operate and maintain HPLC (High-Performance Liquid Chromatography) equipment following analytical methods and protocols.
• Utilize other analytical techniques including UV-Visible Spectrophotometry , Dissolution Testing , and Chromatography .
• Document all testing activities in accordance with Good Documentation Practices (GDP) and GMP guidelines.
• Assist in method validation, system suitability , and instrument calibration.
• Investigate and document any out-of-specification (OOS) or atypical results following established procedures.
• Support laboratory audits and inspections by ensuring complete and accurate laboratory documentation.
• Collaborate with QA, Manufacturing, and Regulatory Affairs teams to ensure consistent quality standards.

Qualifications:

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
• 1–3 years of experience in a QC Laboratory within the pharmaceutical or biotech industry.
• Hands-on experience with HPLC , UV , and Dissolution apparatus is required.
• Familiarity with Chromatographic techniques , GMP regulations, and FDA/ICH guidelines.
• Strong attention to detail, analytical thinking, and problem-solving skills.

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