Scientist I - III

Job Duties Conduct analysis or experiments by following procedures independently. Conduct lot release and stability testing in compliance with GMP/GLP, safety and regulatory requirements to support all development stages. Develop and execute experimental plans of limited scope (e.g., method development, characterization studies, instrument qualification) with minimum supervision. Assist in developing and validating moderately complex analytical methods to test raw materials, intermediates and final products, or quantify biomarkers in biological matrices. Help improve existing complex methods with supervision. Analyze and interpret complex data following procedures. Learn and apply basic GMP/GLP principles. Review test records according to procedures. Maintain laboratory safety and alertness for the safety of coworkers and visitors. Education and/or Job Experience BS with a minimum of 5 years, or MS with a minimum of 3 years of relevant pharmaceutical or biotechnology development experience. Preferred Qualifications Working knowledge of biophysical techniques and analytical characterization of peptides and proteins. Experience supporting formulation and process development. Aseptic processing experience. Experience authoring/revising SOPs, work instructions, test methods, batch records, validation protocols, development reports, and validation reports. Experience in GLP/GMP regulated environments. Excellent oral and written communication skills. Ability to work as part of a multidisciplinary team. #J-18808-Ljbffr Scorpion Therapeutics