About this opportunity
Neurocrine Biosciences lists this Principal Scientist, Analytical Development (Biologics) opportunity in san diego, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
About the Role:
This position will serve as analytical development lead for multiple projects, with a focus on Biologics including monoclonal antibodies, bi‑specific monoclonal antibodies, tri‑specific monoclonal antibodies, and antibody conjugates. Guide analytical activities related to drug substance and drug product development from preclinical through commercial phase. Develop, establish, and validate/qualify analytical methods used to control in‑process intermediates, drug substance, and drug products. Contribute to the development and implementation of control strategies. Responsible for keeping work in compliance with cGMP, safety, and regulatory requirements. Participates in analysis and evaluation of material and products at all stages of development process. Monitors and evaluates completion of tasks and projects.
Your Contributions (include, but are not limited to):
Lead analytical method development and validation/qualification activities for Biologics (e.g. monoclonal antibodies, bi‑specific monoclonal antibodies, tri‑specific monoclonal antibodies, and antibody conjugates) within cGMP compliance in support of preclinical through commercialization
Represent Analytical development on cross‑functional teams
Maintain accountability for analytical deliverables and progress on CMC and manufacturing plans for all development projects
Direct laboratory work and/or lab personnel within the company and at external vendors
Deep technical expertise in separation method development (e.g. SEC‑UPLC, RP‑UPLC, HILIC‑UPLC, IEX‑UPLC, HIC‑UPLC, Mixed Mode‑UPLC, 2D‑LC, CE‑SDS, iCIEF etc.), potency method development (e.g. ELISA, cell‑based bioassay etc.), process related impurities method development (e.g. ELISA, qPCR, LC) for Biologics and extensive knowledge of CQA assessment, analytical comparability, and stability
Support off‑site analytical method transfers, manufacturing support, and interaction with external vendors
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
Requirements:
BS/BA in Analytical Chemistry or related discipline and 8+ years of experience in the analytical/pharmaceutical development field
Experience in method transfer in Analytical Chemistry OR MS/MA in Analytical Chemistry or related discipline and 6+ years of experience OR PhD in Analytical Chemistry or related discipline and 4+ years of relevant experience; may include postdoc experience
Expert knowledge and understanding of Biologics analytical development and a thorough understanding of bioprocess as well as formulation development
Expert knowledge of Biologics extended characterization, critical quality attribute (CQA) assessment, and structure functional relationship
Expert knowledge of Biologics stability study
Extensive experience and expertise with Biologics focusing on analytical method development including but not limited to release/stability method development
Proficient in characterization of Biologics (e.g. monoclonal antibodies, antibody conjugates) using various modern technologies. They may include but not limited to size exclusion liquid chromatography, reverse phase liquid chromatography, hydrophilic interaction liquid chromatography, ion exchange liquid chromatography, hydrophobic interaction liquid chromatography, mixed mode liquid chromatography, UPLC/HPLC, capillary electrophoresis (Maurice/PA800+), imaged capillary isoelectric focusing (Maurice), gel electrophoresis, mass spectrometry, ELISA, bioassays, and molecular analysis
Method development, validation, qualification, and transfer experience in Analytical Development
Comprehensive understanding of cGMP requirements in drug substance and drug product
Expert knowledge of cross‑functional understanding related to drug development
Extensive knowledge of FDA, EMA, WHO, and ICH regulatory requirements and experience in IND/IMPD regulatory filing
Excellent interpersonal skills with strong oral and written communication abilities
Excellent project management skills
Neurocrine 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 $156,900.00-$214,000.00. 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.
We are a top place to work.
Neurocrine Biosciences was named one of the FORTUNE Best Workplaces in Biopharma™ 2025. We were also named a Great Place to Work® Certified company. ©2025 Fortune Media IP Limited. All rights reserved. Used under license.
Our Values:
PASSION: We are driven and love what we do. We are committed to our goals and to making a difference.
INTEGRITY: We do the right thing for patients and our community. We take accountability. We speak up.
COLLABORATION: We trust one another. We are inclusive. We are respectful. We are transparent. Together we succeed.
INNOVATION: We seek and create optimal solutions.
TENACITY: We do not quit. We adapt. We accomplish what others cannot.
Come join our team during this exciting time of growth and opportunities!
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.