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

About the Role:

The Scientific Director, CMC Quantitative Sciences is a senior technical individual contributor responsible for designing and advancing data-driven development and lifecycle management initiatives for drug products, including knowledge management, through application of advanced statistical analysis, experimental design, and quantitative modeling.
Embedded within Pharmaceutical Development, this role serves as the portfolio-level statistical authority supporting drug product development programs from post-Proof of Concept through regulatory submission and the commercial lifecycle.
In addition to serving as a quantitative authority, this role actively supports formulation and process development strategy by integrating statistical and mechanistic understanding of product design (at first principles-level) to optimize formulations for performance, stability and manufacturability, and strengthen process robustness.
The Director partners cross-functionally with Pharmaceutical & Analytical Development, Quality, Regulatory CMC, and Commercial Manufacturing & Supply Chain to ensure that development and manufacturing decisions are supported by rigorous statistical analysis and defensible interpretation of CMC data.
This role provides technical leadership across multiple development programs, strengthening process understanding, enabling robust control strategies, and improving the quality and regulatory defensibility of CMC submissions.
While embedded in Pharmaceutical Development, the position influences programs spanning late-stage development through commercial lifecycle management and serves as a technical authority and mentor for quantitative approaches across CMC functions.

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

Pharmaceutical Development (CMC)

• Owns drug product design and development strategy

• Generates, maintains and leverages process understanding and development data

• Informs control strategy for regulatory submission and hands-off to commercial

Commercial Manufacturing

• Owns routine manufacturing execution and maintains continuity of supply to the market

• Owns site-level monitoring and operational performance

• Owns CPI/CPV strategy, including design, oversight of execution, monitoring and reporting

Scientific Director, Pharmaceutical Development Quantitative Sciences (This Role)

• Provides advanced statistical analysis and modeling expertise across CMC programs

• Translates complex development and manufacturing data into actionable technical insights

• Ensures statistical rigor and regulatory defensibility of CMC data packages

• Serves as a technical authority for statistical interpretation across lifecycle stages

• Supports formulation and process development strategies through data-driven insights and mechanistic interpretation

• Supports troubleshooting efforts and root-cause investigations as needed on both the formulation and process development fronts for development and commercial assets

Complex Data Interpretation

• Apply multivariate tools to support identification of CMAs, CPPs, and design space boundaries

• Serve as a technical authority for complex data interpretation across CMC programs

• Provide statistical guidance for investigations involving process variability. Support root cause analysis of complex development or manufacturing trends

• Integrate datasets across development, analytical, and manufacturing functions to generate actionable insight

• Translate experimental data into formulation and process understanding, including identification of critical material attributes, excipient functionality, and process sensitivities

• Support development teams in interpreting DoE outcomes to refine formulations and unit operations (e.g., granulation, blending, compression, coating)

• Formulation & Process Development Support

• Partner with Pharmaceutical Development scientists to design and optimize formulations using structured experimental approaches (DoE, mixture designs, response surface methods)

• Provide quantitative and mechanistic input into selection of excipients, formulation composition, and process parameters

• Support development and scale-up of key unit operations (e.g., fluid bed granulation, roller compaction, blending, tableting, coating) through data-driven modeling and risk assessment

• Guide process characterization strategies, including definition of parameter ranges, interaction effects, and scale dependencies

• Contribute to development of robust manufacturing processes by linking material attributes, process parameters, and product performance

• Support assessment of formulation and process robustness, including sensitivity analyses and failure mode identification

Regulatory Submission Support

• Serve as a primary statistical authority supporting CMC regulatory submissions (NDA, BLA, MAA)

• Ensure statistical methodologies used in development and validation are regulatory defensible and aligned with ICH guidelines (Q8, Q9, Q10, Q14)

• Provide statistical interpretation for process validation strategies and control strategy justification

• Support responses to regulatory questions related to CMC data analysis and statistical methodology

• Contribute to justification of formulation composition, process design, and design space within regulatory filings

Capability Building

• Strengthen quantitative capabilities across Pharmaceutical Development

• Drive adoption of modern data science and modeling approaches that improve development efficiency and process understanding

• Establish best practices for experimental design and statistical analysis in development programs

• Mentor scientists on statistical thinking and interpretation of experimental results

• Promote integration of statistical and formulation/process science to enable more predictive and efficient development approaches

Requirements:

• PhD, PharmD, or MS in Statistics, Chemical Engineering, Pharmaceutical Sciences, or related quantitative discipline

• 12-15+ years of experience applying statistical analysis to pharmaceutical development or manufacturing at all stages of development

• Demonstrated expertise in:Design of Experiments (DoE), multivariate analysis, process capability and variability analysis, statistical modeling of manufacturing processes

• Working knowledge of formulation principles and solid oral dosage formulation and unit operations (e.g., granulation, blending, encapsulation, compression, coating) required. Hands-on experience is strongly preferred

• Experience supporting late-stage development and regulatory submissions (IND/IMPD/CTA/NDA/BLA/MAA)

• Proficiency with analytical platforms such as JMP, R, Python, or equivalent statistical tools

• Strong ability to influence cross-functional teams through technical expertise and data interpretation

This role:

• Act as a portfolio-level technical authority for quantitative approaches throughout the drug product lifecycle. Mentor scientists and strengthen quantitative capabilities within Pharmaceutical Development

• Guide experimental design, process characterization, and control strategy development

• Actively influence formulation and process development decisions through data-driven and mechanistic insights

• Support regulatory submissions (NDA, BLA, MAA) with defensible statistical methodology

• Integrate datasets across development, analytical, and manufacturing functions for program-level insight

• Provide advanced statistical analysis, modeling, and interpretation across CMC development programs

• Translate complex development, analytical, and manufacturing data into actionable technical insights

• Ensure statistical rigor and regulatory defensibility of CMC data packages and submissions

• Promote adoption of modern data science and modeling approaches to improve efficiency and process understanding

This role does not:

• Directly manage or formally supervise staff

• Own routine manufacturing execution or site-level operational performance

• Serve as program CMC functional area lead, make final operational, business, or budgetary decisions for CMC programs

• Manage headcount, administrative processes, or team performance evaluations

• Replace hands-on experimental or process work performed by development teams

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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 $0.00-$0.00. 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 35% 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.