Job Details

ID #54179779
Estado Pennsylvania
Ciudad Lancaster
Tipo de trabajo Full-time
Salario USD TBD TBD
Fuente Eurofins
Showed 2025-07-17
Fecha 2025-07-17
Fecha tope 2025-09-15
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Scientist I- Med Device Microbiology

Pennsylvania, Lancaster, 17601 Lancaster USA
Aplica ya

Perform various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running a variety of equipment or instrumentation independently; working efficiently; ensuring that client receives quality data by reviewing laboratory data for accuracy, clarity and adherence to GMP and/or GLP regulations; evaluate current systems and suggest process improvements when appropriate; initiate and assist completing investigations.Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Demonstrates and promotes the company vision Demonstrates strong client service skills, teamwork, and collaboration Proactively plans and multitasks to maximize productivity Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Regular attendance and punctuality Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision Perform/review preparations of reagents, samples, and standards according to procedures. Perform or review routine and non-routine analyses; instrumental analyses; including calibration and troubleshooting of instruments independently Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors Understand and perform calculations as required by test methods Understand and utilize computers for information access, calculations, and report preparation/reviewRead and understand analytical procedures (compendial and client supplied) and internal SOP's Demonstrate technical writing skills Process/review data, generate/review reports, and evaluate data Communicate effectively, both orally and in writing Independently seek out work Perform laboratory maintenance as required Commitment to occasional overtime as workload requires Support LEAN initiatives Conducts all activities in a safe and efficient manner Communicates effectively with client staff members Ensures good housekeeping with a neat, clean and orderly workspace Performs other duties as assigned

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