Scientist II, Analytical Development

Neurocrine Continental; San Diego (CA); On-site; USD 110,000 - 150,000; Full time

Job summary

Neurocrine Biosciences is seeking an analytical development scientist II to lead development activities for small molecule drug substances from preclinical through commercial stages. The role focuses on analytical chemistry, method development/validation, and regulatory documentation support.

The candidate will supervise lab personnel, oversee external CRO/CDMO analytical work, and collaborate across CMC, Quality, Regulatory, and Manufacturing to ensure product readiness and successful

Qualifications

• BS/BA degree in chemistry or closely related field with 4 years of pharma analytical experience.
• MS/MA degree in chemistry or closely related field with 2 years of relevant experience; or PhD with some experience.
• Demonstrates solid understanding of project/group goals and methods; can explain data implications.
• Strong knowledge of scientific principles, methods and techniques.
• Experienced with analytical chemistry projects from preclinical through commercialization and regulatory input.

Responsibilities

• Lead analytical development to support research, tech transfer and commercialization of drug substance and drug product.
• Provide project management for analytical in support of Chemical and Product Development projects.
• Analyze and evaluate materials and products across development stages.
• Supervise lab work and personnel; ensure safe laboratory practices.
• Contribute to CMC regulatory documentation and development of lab policies.

Skills

Analytical development

Method development/validation

Project management

Cross-functional collaboration

Data interpretation

Education

BS/BA in chemistry

MS/MA in chemistry

PhD in chemistry

Tools

Laboratory equipment/tools

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. For more information, visit neurocrine.com , and follow the company on LinkedIn , X , Facebook and YouTube . ( *in collaboration with AbbVie )

About the Role:

Responsible for analytical development activities for small molecule drug substances from preclinical through commercial phase. This role is laboratory‑focused, requiring deep expertise in analytical chemistry and strong problem‑solving skills. With supervision, the scientist II independently provides support to analytical activities including development, execution, validation, transfer and troubleshooting of methods used to control raw materials, in‑process, intermediates and final products. While also participate overseeing analytical work performed at external CROs and CDMOs. Conducts work in compliance with cGMP, safety, and regulatory requirements. The position works cross‑functionally with teams across CMC, Technical Operations, Quality, Regulatory Affairs, Manufacturing, and external partners to support product development, manufacturing readiness, and regulatory submissions. The role also contributes to overall control strategy development and ensures scientific and technical alignment through all phases of product development. _

Your Contributions (include, but are not limited to):

• Responsible for analytical development to support research and development, tech transfer and commercialization of drug substance and drug product processes, as well as oversight of batch testing/release and regulatory document contribution through managerial and individual input
• Provides project management for analytical in support of Chemical and Product Development projects
• Provides analysis and evaluation of material and products at all stages of the development process
• Monitors and evaluates completion of tasks and projects
• Plans and manages projects
• Represents Analytical Chemistry on cross‑functional teams
• Maintains accountability for analytical deliverables and progress on R&D and manufacturing plans for all development projects
• Independently designs, plans and executes activities towards the goals of one or more analytical chemistry projects to support pre‑clinical through commercial activities
• Supervises laboratory work and/or lab personnel and ensures safe laboratory practices
• Performs analytical development and optimizes methods in support of preclinical through commercialization
• Creates and implements novel ideas and techniques to support analytical activities with Chemical and Product Development
• Provides support for off‑site analytical transfers, manufacturing support and interaction with contractors
• Provides input into CMC regulatory documentation and supporting work
• Provides effective supervision of laboratory personnel and guidance for their professional development
• Contributes to development of policies and department strategies
• Builds and enhances internal and external professional relationships
• Effectively see projects to completion
• Understands how to effectively negotiate, persuade, and influence
• Other duties as assigned

Requirements:

• BS/BA degree in chemistry or closely related field and 4 years of experience in the pharmaceutical industry, focusing on analytical chemistry
• Extensive hands‑on experience in pharmaceutical analysis, methods development/validation for various active ingredients and/or dosage forms
• MS/MA degree in chemistry or closely related field and 2 years of similar experience noted above OR
• PhD or equivalent in chemistry or closely related field and some relevant experience; may include postdoc experience
• Demonstrates solid level of understanding project / group goals and methods
• Able to explain the process behind the data and implications of the results
• Strong knowledge of one or more scientific disciplines, becoming expert in one discipline
• Strong knowledge of scientific principles, methods and techniques
• Strong knowledge and demonstrated ability working with a variety of laboratory equipment/tools
• Ability to work as part o