Scientist II, CMC Downstream Process Development

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:

Drive the progression of assigned development programs by applying independent scientific judgement to complex technical challenges. This role deepens mechanistic understanding of processes, translates experimental data into clear scientific rationale, and influences project-level decisions that shape development strategy. As a trusted technical contributor, collaborate across functions, strengthen regulatory alignment, and play a key role in advancing assets toward clinical and commercial milestones. _

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

Apply scientific or engineering principles with increasing complexity to process development lifecycle activities

Independently evaluate scientific data and recommend development decisions balancing product understanding and risk

May lead defined process scale-up and technology transfer initiatives

Support project planning and advancement within cross-functional teams

Maintain accountability for assigned development deliverables

Contribute to risk assessments and mitigation strategies

Independently design, execute, and interpret studies supporting project objectives

Ensure laboratory and pilot-scale work is efficient, compliant and aligned with safety standards

Identify process challenges and lead troubleshooting and optimization activities

Recommend new technologies or methods to improve product quality and process performance

Assist in managing contract manufacturing activities

Contribute to CMC documentation and regulatory readiness efforts

Mentor junior scientists and support team development

Perform other duties as assigned

Requirements:

BS/BA degree in chemistry, biochemistry, biology, or similar scientific discipline AND 4+ years of relevant experience OR

MS/MA degree in chemistry, biochemistry, biology, or similar scientific discipline AND 2+ years of relevant experience OR

PhD in chemistry, biochemistry, biology, or similar scientific discipline AND some years relevant experience; may include postdoc experience

Well-developed understanding of process development approaches and scale-up strategies

Strong laboratory and productivity skills

Manufacturing experience internally or with external partners

Good understanding of cGMP and regulatory requirements

Demonstrated cross-functional understanding related to drug development

Strong proficiency with laboratory equipment and tools

Strong knowledge of scientific or engineering principles and methods

Demonstrated ability to interpret complex data sets and articulate scientific rationale

Consistently recognizes anomalous results and determines appropriate next steps

Explains data implications clearly to cross-functional stakeholders

Builds effective internal and external working relationships

Detail oriented with strong analytical thinking

Works effectively as part of a team and may lead defined activities

Strong communication skills

Understands broader scientific impact on project outcomes

Manages multiple deadlines with accuracy and efficiency

Demonstrates developing project leadership skills

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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 $110,800.00-$151,000.00. 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 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.