Principal Scientist, Analytical Development
- California, Maryland, United States
- California, Maryland, United States
À propos
At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.
What We Do:Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, 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 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 , and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)
About the Role: This position serves as the analytical lead for multiple projects, with a focus on gene therapy and biologics. The role guides analytical activities supporting drug substance and drug product development from preclinical through commercial phases. Responsibilities include developing, establishing, and validating or qualifying analytical methods to control raw materials, in-process materials, intermediates, and drug substance and product. The position contributes to the development and implementation of control strategies, with an emphasis on advancing innovative analytical techniques. The role also ensures compliance with cGMP, safety, and regulatory requirements, and supports the analysis and evaluation of materials and products at all stages of the development process. Additionally, the position monitors progress and evaluates the completion of assigned tasks and projects._
Your Contributions (include, but are not limited to):Lead analytical development and characterization activities for multiple projects with focus on gene therapy and biologic compounds, Represent Analytical development on cross-functional teams. Maintain accountability for analytical deliverables and progress on CMC and manufacturing plans for all development projects
Design, plan, and execute activities towards the goals of one or more analytical development projects to support pre-clinical through commercial activities
Execute characterization of gene therapy and biologic modalities using high-resolution mass spectrometry, chromatographic separations, and other biophysical methodologies.
Perform laboratory work and/or direct lab personnel within the company and at external vendors
Ensure safe laboratory practices
Perform analytical development and methods optimization in support of preclinical through commercialization
Create and implement novel concepts and techniques to support analytical activities with Chemical and Product Development
Support off-site analytical transfers, manufacturing support, and interaction with contractors
Provide input into CMC regulatory documentation and supporting work
Leverage literature, ICH/ Regulatory guidance, and practical experience to perform this work and influence CMC strategies
Contribute to development of policies and department strategies
Build and enhance internal and external professional relationships
Support career development and technical growth of team members
Present finding at varying levels across the company
Other duties as assigned
BS/BA and 12+ years of experience, or OR
MS/MA and 10+ years of experience, or OR
PhD or equivalent and 4+ years of relevant experience
Expert knowledge and understanding of analytical chemistry, bioanalysis, and a thorough understanding of bioprocess as well as formulation development
Method development, validation, and
Compétences linguistiques
- English
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