- Jayuya, Puerto Rico, United States
- Entry
- 3–5 years
Perform chemical analyses and support quality control processes in a pharmaceutical manufacturing environment.
Responsibilities
- Perform chemical analyses of raw materials, in-process samples, water systems, intermediates, and finished products in accordance with approved methods and specifications.
- Execute specialized analytical testing using laboratory instrumentation such as HPLC, UV/Vis Spectrophotometry, pH Meters, Infrared, Atomic Absorption, Karl Fischer, TOC Analyzer, Polarimeter, and related equipment.
- Evaluate test results against established product specifications and make sound analytical assessments to support product quality decisions.
- Perform analytical data review to ensure accuracy, completeness, and compliance with regulatory requirements.
- Follow current Good Manufacturing Practices (cGMP), Good Documentation Practices (cGDP), and Good Laboratory Practices (cGLP) in all laboratory activities.
Requirements
- Bachelor's Degree in Chemistry or a related scientific discipline
- Nice to have: Bilingual in English and Spanish