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Senior Scientist, Analytical Development (Small Molecule

Job in San Diego, San Diego County, California, 92101, USA
Listing for: Avery Healthcare Group Ltd.
Full Time position
Listed on 2026-08-10
Job specializations:
  • Science
    Pharmaceutical Science/ Research, Research Scientist, Medical Science, Clinical Research
Job Description & How to Apply Below
Position: Senior Scientist, Analytical Development (Small Molecule)

Senior Scientist, Analytical 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 patients with 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.

The Senior Scientist, Analytical Development, is 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. The Senior Scientist independently manages analytical activities for assigned programs including development, execution, validation, transfer and troubleshooting of methods used to control raw materials, in-process, intermediates and final products.

While also 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):
Perform development and optimization of phase-appropriate analytical methods for starting materials, intermediates, and drug substances to support programs from early development through commercialization using techniques such as HPLC, GC, MS, IC, FTIR, UV, NMR, KF and other relevant techniques to ensure method suitability for intended purpose Perform analytical method verification and validation within cGMP compliance and in accordance with regulatory guidelines Perform analytical development activities for the characterization of small molecules utilizing various chemical-physical characterization techniques Perform development stability studies, forced degradation studies and support impurity identification Independently lead and execute analytical development activities and contribute to overall control strategy for assigned projects Provide scientific leadership and technical support for quality investigations, including OOS/OOT events, deviations, root cause analyses, and CAPAs Maintain accurate and comprehensive laboratory documentation in compliance with company procedure Represent Analytical development on cross-functional teams.

Maintain accountability for analytical deliverables and progress on CMC and manufacturing plans for all development projects Conduct laboratory work independently and/or train lab personnel within the company and at external vendors Support CMC regulatory documentation and filings as needed Support off-site analytical transfers, manufacturing support, and interaction with contractors Clearly communicate analytical results, risks, and recommendations through high-quality technical reports, presentations, and cross functional discussions across the company Ensure safe laboratory practices Create and implement novel concepts and techniques to support analytical activities with Chemical and Product Development Contribute to development of policies and department strategies Partner closely with other team…

Position Requirements
10+ Years work experience
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