Employee Responsibilities:Perform physical, chemical, and instrumental analysis of raw materials, active pharmaceutical ingredients and/or finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels)Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGA, DSC, auto-titrators, and TLC.Prepare samples and standards for analysis while running some instrumentation with minimum supervision.Perform monthly maintenance of laboratory equipment.Document and review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate.Determine if data is compliant, defendable, and of sound quality based on industry regulations and methodology.Review methods to ensure procedures are followedSet up and validate new analytical or related processes used by the departmentPerform strategic data analysis and identify patterns to improve metrics.Write and review laboratory investigationsAuthorize written reports (e.g., SOP, OMC, client reports)
Job Details
ID | #53370137 |
Estado | Pennsylvania |
Ciudad | Lancaster |
Tipo de trabajo | Full-time |
Salario | USD TBD TBD |
Fuente | Eurofins |
Showed | 2025-01-30 |
Fecha | 2025-01-30 |
Fecha tope | 2025-03-31 |
Categoría | Etcétera |
Crear un currículum vítae | |
Aplica ya |
Associate Scientist - Data Reviewer
Pennsylvania, Lancaster, 17601 Lancaster USA