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Sr. Scientist, CMC Upstream Gene Therapy Development

Neurocrine Biosciences
United States, California, San Diego
May 13, 2025
Who We Are:

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 Biosciencesis 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, visitneurocrine.com, and follow the company onLinkedIn,XandFacebook. (*in collaboration with AbbVie)

About the Role:

Responsible for pre-clinical and clinical phase scientific process research and development for gene therapy and/or antibody modalities, including internal development and manufacture of GLP and support for external manufacture of GMP drug substance. Significant upstream and/or downstream laboratory contributions required to enable drug substance process optimization to ensure robust delivery of the Neurocrine pipeline. Position also entails regulatory awareness and document contribution, quality and cGMP knowledge, and an ability to work with cross-functional and external partners. May provide project leadership or support for CMC programs and may lead work streams or platform projects within Chemical Development. May manage and mentor other scientists and/or team members.

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Your Contributions (include, but are not limited to):
  • Supports project planning efforts. Participates on cross-functional teams representing Chemical Development

  • Maintains accountability for assigned deliverables for R&D and manufacturing plans for Chemical Development projects

  • Independently plans and executes activities towards the goals of one or more project work streams to support Chemical Development Programs

  • Ensures laboratory work is done productively and practices safe laboratory skills

  • Performs process R&D and optimizes drug substance processes

  • Recommends alternatives, performs research towards new methods and techniques to solve problems

  • Assists with managing off-site synthesis, manufacturing activities and may interact with contractors

  • May provide input for portion(s) of CMC regulatory documentation and supporting work

  • May train lower-level scientists and/or team members

  • Builds and enhances internal and external professional relationships

  • Other duties as assigned

Requirements:
  • BS/BA degree in Chemistry, chemical engineering, or other similar scientific fieldand 4+ years of experience in experience in pharmaceutical/process development field, including API manufacturing experience OR

  • MS/MA degree in Chemistry, chemical engineering, or other similar scientific field and 3+ years of similar experience above OR

  • PhD in Chemistry, chemical engineering, or other similar scientific field and 2+ years relevant industry experience; may include postdoc experience

  • Consistently recognizes anomalous and inconsistent results and interprets experimental outcomes

  • Able to explain the process behind the data and implications of the results and plan next steps

  • 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 of a team; may train lower level scientists

  • Strong communications, problem-solving, analytical thinking skills

  • Detail oriented yet can see broader picture of scientific impact on team

  • Ability to meet multiple deadlines, with a high degree of accuracy and efficiency

  • Ability to build and manage internal and external working relationships

  • Strong understanding of gene therapy and/or antibody development and manufacture

  • A well-developed understanding of biologics (upstream and/or downstream) as well as current techniques and literature

  • Strong laboratory and productivity skills

  • Drug substance manufacturing experience both internal and with external partners

  • Good understanding of cGMP requirements and regulatory aspects of biologics

  • Demonstration of cross-functional understanding related to drug development

#LI-DM1

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.

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The annual base salary we reasonably expect to pay is $108,600.00-$157,350.00. 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 20% 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.
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