Who We Are: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 challengesServe as the primary scientific decision-maker for assigned assetsLead process scale-up and technology transfer initiatives, proactively managing technical riskPlan and manage scientific activities; represent development in cross-functional teamsMaintain accountability for asset-level deliverables and production planning.Lead technical risk assessments to support project advancementIndependently design and oversee advanced activities supporting clinical through commercial developmentSupervise laboratory and pilot-scale work and ensure safe laboratory practicesIdentify and resolve significant process challenges using data-driven approachesRecommend innovative solutions to improve product quality and manufacturing consistencyManage contract manufacturing activities and contractor relationshipsProvide scientific leadership in CMC regulatory documentationContribute to development of departmental scientific policies and standardsMentor scientists and support professional developmentBuild and strengthen internal and external professional relationshipsPerform other duties as assignedRequirements:BS/BA in chemistry, biochemistry, biology, or similar scientific discipline OR chemical engineering, biochemical engineering, or similar engineering discipline AND 12+ years of experience in experience in pharmaceutical/process development field, including API manufacturing person in plant activities, Experience managing laboratory, maximizing productivity is desirable. ORMS/MA in chemistry, biochemistry, biology, or similar scientific discipline OR chemical engineering, biochemical engineering, or similar engineering discipline AND 10+ years of similar experience noted above ORPhD in chemistry, biochemistry, biology or similar scientific discipline OR chemical engineering, biochemical engineering, or similar engineering AND 4+ years of relevant experience; may include postdoc experienceBroad and deep knowledge of scientific or engineering principles with subject matter expertiseRecognized authority capable of defending scientific strategyDevelops creative and effective solutions to technical challengesUnderstands interdependencies across functional areasLeads multiple teams or initiativesDemonstrates strong leadership and mentoring skillsExcellent communication and analytical skillsUnderstands impact across multiple programs and departmentsManages multiple priorities with high accuracyStrong project management skillsThorough understanding of process development and scale-up strategiesExcellent laboratory and productivity skillsKnowledge of validation and control strategy developmentManufacturing experience internally and externallyStrong understanding of cGMP and regulatory requirementsDemonstrated cross-functional drug development knowledgeAdvanced proficiency with laboratory equipment and tools#LI-LS1Neurocrine Biosciences is an EEO/Disability/Vets employer. We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description._The annual base salary we reasonably expect to pay is $130,800.00-$179,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.