Descripción del Empleo:
Performs all laboratory analysis and activities in accordance with cGMP's practices, Internal and external regulations and policies, and consistent with supply chain cycle time goals. Responsible for following laboratory priority report and in-process boards to support manufacturing rhythm wheels and business rules. Complies with all Laboratory Schedules for raw materials and/or drug product testing and special projects. Assures to follow Lean QA initiatives and requirements. Operates all laboratory equipment and instrumentation required for testing such as UV-Visible/IR spectrophotometers, pH meters, viscometers, specific gravity apparatus, analytical balances, polarimeters , GC and HPLC chromatographers, dissolution baths and any other computerized system. Verifies documentation of data generated by other Lab analysts in a timely manner and according to specifications.
Requisitos:
Bachelor Degree in Chemistry At least 1 years related experience in a pharmaceutical laboratory testing. University laboratory or research experience could be validated.
Knowledge/ experience operating all laboratory equipment and instrumentation required for testing such as UV-Visible/IR spectrophotometers, pH meters, viscometers, specific gravity apparatus, analytical balances, polarimeters, Karl Fischer titration, GC and HPLC chromatographers, dissolution baths and any other computerized system
Bilingual English & Spanish. All documentation should be written in English.
Ability to read, analyze, and interpret common scientific and technical journals
Ability to write speeches and articles for publication that conform to prescribed style and format.
Knowledge of Microsoft Office applications. Basic knowledge of applications such as LIMS, TrackWise, SAP and EMPOWER.