Associate Scientist, Analytical Development

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit  neurocrine.com , and follow the company on  LinkedIn ,  X , Facebook and YouTube . ( *in collaboration with AbbVie ) About the Role: Under direct supervision, is responsible for development and execution of analytical test methods that facilitate drug product development / manufacturing and regulatory submissions for clinical study introduction through phase III trials. Activities includes test method development, qualification/validation, transfer and execution. Supports late stage troubleshooting and development of products, processes, and methods in support of product commercialization. _ Your Contributions (include, but are not limited to): With direct supervision, develops and executes chemical and instrumental methods (e.g. HPLC, GC, TGA, DSC, MS, FTIR, Water Content) of analyses of drug product development compounds Accurately follows established test methods, procedures, and pharmacopeia chapters (e.g. Dissolution, Content Uniformity) to generate data essential for strategic decision making With direct supervision, plans and executes forced degradation, informal stability, and excipient compatibility studies With direct supervision and as appropriate, assists/leads the development of analytical methods, investigations for out of specification, out of trend, and/or anomalous results With direct supervision, collaboratively plans and executes cross functional studies for formulation development Recognizes and responds to unexpected or anomalous observations in all activities Maintains complete and accurate records of laboratory work in conformance with company SOPs and training Provides detailed reviews of peer generated data as well as that generated from contracted service providers Other duties as assigned Requirements: BS/BA degree in chemistry or closely related field and some relevant industry experience preferred; Experience with Empower a plus Working knowledge of data systems for computer-controlled instrumentation Familiarity with performing analytical testing of solid oral drug products; Hands-on knowledge preferred Knowledge of conducting HPLC analysis and troubleshooting. Working knowledge of performing stability indicating method development a plus Familiarity with performing dissolution analysis and troubleshooting. Hands-on knowledge performing dissolution method development a plus Understanding of analytical data evaluation and ability to draw meaningful conclusions Ability to present analytical data clearly and demonstrate knowledge of the testing and the product Knowledge of cGMP expectations for laboratory records and quality systems Knowledge of ICH guidance and common testing per USP chapters Knowledge of statistical analysis a plus Ability to provide ideas for process improvements Able to execute experiments efficiently and suggest small process improvements Able to recognize patterns or inconsistencies in data results Able to deduce meaningful results while conducting