Senior Scientist, CMC Downstream Process 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: Serve as the scientific leader for assigned assets, shaping development strategy through deep process understanding and ensuring regulatory defensibility of key decisions. Combines advanced technical expertise with cross-functional influence, guiding asset progression from early development through commercialization. As the primary scientific authority for your programs, define technical direction, lead critical risk assessments, and ensure that scientific rigor guides lifecycle strategy and manufacturing readiness. _ Your Contributions (include, but are not limited to): Apply advanced scientific or engineering principles to complex process development challenges Serve as the primary scientific decision-maker for assigned assets Lead process scale-up and technology transfer initiatives, proactively managing technical risk Plan and manage scientific activities; represent development in cross-functional teams Maintain accountability for asset-level deliverables and production planning. Lead technical risk assessments to support project advancement Independently design and oversee advanced activities supporting clinical through commercial development Supervise laboratory and pilot-scale work and ensure safe laboratory practices Identify and resolve significant process challenges using data-driven approaches Recommend innovative solutions to improve product quality and manufacturing consistency Manage contract manufacturing activities and contractor relationships Provide scientific leadership in CMC regulatory documentation Contribute to development of departmental scientific policies and standards Mentor scientists and support professional development Build and strengthen internal and external professional relationships Perform other duties as assigned Requirements: BS/BA in chemistry, biochemistry, biology, or similar scientific discipline OR chemical engineering, biochemical engineering, or similar engineering discipline AND 6+ years of experience in experience in pharmaceutical/process development field, including API manufacturing person in plant activities, Experience managing laboratory, maximizing productivity is desirable. OR MS/MA in chemistry, biochemistry, biology, or similar scientific discipline OR chemical engineering, biochemical engineering, or similar engineering discipline AND 4+ years of similar experience noted above OR PhD in chemistry, biochemistry, biology or similar scientific discipline OR chemical engineering, biochemical engineering, or similar engineering AND 2+ years of relevant experience; may include postdoc experience Broad and deep knowledge of scientific or engineering principles with subject matter expertise Recognized authority capable of defending scientific strategy Develops creative and effective solutions to technical