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.

Contract work,