The QC Analyst I performs Analytical chemistry examination testing on raw materials, finished products or stability samples in accordance with approved Standard Operating Procedures (SOPs) and valid methods.
Key Responsibilities
Chemical or Physical testing analysis of raw materials, finished products, stability or request samples
Documenting and submitting all raw data and results in LIMS
Preparation of reagents for chemical analysis including peer review
Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR
Qualifications
Bachelor's degree in chemistry, biology, microbiology or other related science with relevant laboratory coursework is required.
0 - 2 years laboratory experience, preferably in a GMP environment
Wet Chemistry testing, Balance, Dissolution, FTIR, KFM, UV/Vis, Titrations, Viscosity, PSD testing, pH, conductivity
Strong written, verbal, and interpersonal communication skills
Proficiency with computer software such as MS Word, Excel, or PowerPoint