Responsibilities: of the Scientist I: • Perform analytical sample preparation and extraction of target analytes from raw material and finished product matrices utilizing dilution, filtration, centrifugation, and multi-step extraction techniques. • Execute analytical testing using HPLC, GC, and related instrumentation while evaluating extraction efficiency, sample recovery, and matrix interferences. • Author, execute, and summarize method verification, validation, and method transfer protocols and reports in accordance with USP <1225>, USP <1226>, and ICH Q2(R2) guidelines. • Utilize Empower chromatography software for data acquisition, processing, reporting, and audit trail review. • Maintain complete cGMP documentation including laboratory notebooks, SOP compliance, data review, and data integrity requirements. • Support investigations, forced degradation studies, and routine testing of raw materials, in-process samples, and finished products. Qualifications: of the Scientist I: • BS or MS in Chemistry or a related scientific discipline. • 4+ years of pharmaceutical laboratory experience supporting quality control or analytical testing activities. • Hands-on experience with analytical sample preparation, extraction techniques, recovery studies, and troubleshooting matrix-related analytical challenges. • Experience performing and documenting method verifications, method validations, and method transfers within a cGMP environment. • Advanced proficiency with HPLC chromatography and Empower software; Agilent HPLC experience preferred. • Strong knowledge of FDA-regulated laboratory operations, cGMP requirements, USP <1225>, USP <1226>, and ICH Q2(R2). Compensation: for the Scientist I includes: • Compensation: $35 - $40/hr (Depending on Experience) • Comprehensive benefits package including medical, dental, vision, and retirement plans • 6 Month Contract #LI-MM8 #LI-ONSITE
| Location | Greenville, SC |
| Salary | $35–$40 Per Hour |
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