Neurocrine Bioscience - San Diego, CA

posted 2 months ago

Full-time - Mid Level
San Diego, CA

About the position

The Scientist in Analytical Development at Neurocrine Biosciences is responsible for developing and executing instrumental methods of analysis for various compounds and materials related to drug development. This role involves ensuring compliance with safety and regulatory requirements while conducting analyses and evaluations throughout the development process. The position requires collaboration with cross-functional teams and the ability to maintain accurate laboratory records.

Responsibilities

  • Develops and executes instrumental methods of analyses for development compounds, drug substances, raw materials, intermediates, drug product, and packaging materials.
  • Accurately follows established test methods, procedures, and pharmacopeia chapters to generate essential data.
  • Plans and executes in-house stability studies for drug substances, intermediates, and prototype drug products with supervision.
  • Assists in the development of analytical methods and investigations for out of specification results under supervision.
  • Collaboratively plans and executes cross-functional studies for chemical and formulation development with supervision.
  • Maintains complete and accurate records of laboratory work in compliance with company SOPs.
  • Provides detailed reviews of peer-generated data and data from contracted service providers.
  • Maintains inventory of laboratory consumables and coordinates vendor service calls for instrument maintenance.

Requirements

  • BS/BA degree in chemistry or closely related field and 2+ years of pharmaceutical industry experience in an R&D/QC setting, including conducting HPLC analysis.
  • MS/MA degree in chemistry or closely related field preferred with some similar industry experience.
  • PhD in chemistry or closely related field with relevant experience is a plus.
  • Proficient in using MS-Excel and MS-Word, as well as data systems for computer-controlled instrumentation.
  • Practical working knowledge of conducting HPLC analysis and troubleshooting.
  • Knowledge of cGMP expectations for laboratory records and quality systems.
  • Strong knowledge of one scientific discipline and good knowledge of scientific principles, methods, and techniques.

Nice-to-haves

  • Experience in project management.
  • Ability to provide ideas for process improvements.
  • Strong communication and problem-solving skills.

Benefits

  • Competitive salary range of $109K - $138K per year.
  • Inclusive and positive company culture.
  • Opportunities for professional development.
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