Assistant Technical Operations Manager Jobs in California

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) At Neurocrine, strong leadership drives both business results and team success. We look for leaders who think strategically, anticipate what’s ahead and set clear direction, while building and empowering high‑performing teams. Successful leaders foster an environment where people are motivated to do their best work and deliver meaningful, measurable impact through sound decision‑making and accountability. About the Role:

About the Role:

The Program Manager, Technical Operations supports the planning, execution, and operational effectiveness of Technical Operations programs across the development portfolio. The role provides program management leadership for complex, multidisciplinary initiatives and serves as a key operational partner to CMC functional leaders, program teams, and cross‑functional stakeholders.

The Program Manager is responsible for translating program objectives into integrated execution plans, establishing effective governance, and operating rhythms, identifying and managing dependencies and risks, and ensuring transparency and accountability across participating functions.

The role may coordinate six or more technical sub‑teams or workstreams within the scope of an assigned program and ensures that strategy, critical‑path activities, interdependencies, decisions, and emerging risks are clearly communicated to appropriate stakeholders.

This position requires a strong understanding of pharmaceutical development and the interactions among core CMC disciplines, including Drug Substance/API Development, Analytical Development, Drug Product/Pharmaceutical Development, Manufacturing, Supply Chain, Quality, and CMC Regulatory.

The Manager works cross‑functionally with partners in Research, Clinical Development, Regulatory Affairs, Quality, Finance, and other functions to ensure Technical Operations activities support broader program and company objectives.

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

Program and Project Management

Lead the integrated planning and execution of assigned Technical Operations and CMC programs, initiatives, and major workstreams from development planning through key program milestones

Develop, maintain, and communicate integrated program plans, timelines, milestones, critical paths, dependencies, decision points, and key deliverables

Establish and manage appropriate meeting cadences, governance forums, decision logs, action trackers, and status reporting mechanisms

Monitor execution against agreed plans and proactively identify schedule risks, resource constraints, cross‑functional dependencies, and emerging issues

Partner with functional subject‑matter experts to evaluate options, develop mitigation strategies, and support timely resolution or escalation of issues

Facilitate scenario planning and trade‑off discussions to enable informed decisions related to timelines, sequencing, dependencies, and execution priorities

Maintain clear documentation of key program assumptions, decisions, risks, actions, and accountabilities

CMC and Technical Operations Integration

Apply working knowledge of CMC development disciplines—including API/drug substance, analytical development, pharmaceutical/drug product development, manufacturing, supply chain, quality, and regulatory activities—to effectively integrate cross‑functional plans

Understand upstream and downstream impacts of Technical Operations activities and proactively connect interdependent work across functions

Partner with technical leaders to translate functional strategies and technical activities into coordinated program‑level plans and milestones

Facilitate alignment between Technical Operations activities and broader Research, Clinical Development, Regulatory, Quality, and portfolio objectives

Support development and maintenance of integrated CMC strategies, timelines, and readiness plans for key development and regulatory milestones

Serve as the program management representative for assigned Technical Operations initiatives and provide clear, data‑driven recommendations to program and functional leadership

Strategic and Operational Support

Support execution of departmental and functional priorities by translating strategic objectives into clear tactical plans, deliverables, timelines, and ownership

Provide leadership with accurate and timely visibility into program progress, risks, resource constraints, decisions, and key operational considerations

Facilitate departmental, program, or cross‑functional planning sessions and ensure resulting decisions and actions are appropriately documented and followed through

Analyze program information and operating trends to identify near‑term challenges, opportunities, and downstream impacts

Recommend practical changes to operating approaches, processes, or governance mechanisms when they will improve execution or team effectiveness

Contribute to resource and capacity discussions by providing visibility into workload, timing, dependencies, and program priorities

Risk, Issue, and Decision Management

Establish disciplined approaches for identifying, assessing, tracking, and communicating program risks and issues

Work with team members and functional leaders to develop mitigation and contingency plans for material risks

Ensure decisions are supported by relevant data, clearly documented, and translated into updated plans and accountabilities

Recognize when issues require broader leadership involvement and facilitate timely escalation with clear options and recommendations

Monitor the outcomes of significant decisions and adjust plans as necessary to maintain progress toward objectives

Promote a solutions‑oriented team environment in which issues are surfaced early and accompanied by proposed paths forward

Operational Excellence

Identify and implement opportunities to improve program management processes, workflows, governance practices, and cross‑functional collaboration

Standardize fit‑for‑purpose templates, planning approaches, dashboards, metrics, and reporting mechanisms where appropriate

Partner with stakeholders to support adoption of new project management systems, digital tools, data capabilities, and operating practices

Use data and stakeholder feedback to assess effectiveness of existing processes and recommend improvements

Requirements:

6+ years of applicable experience AND Bachelor’s degree OR 4+ years of applicable experience AND Master’s degree OR 2+ years of applicable experience AND PharmD, or PhD

Direct experience supporting CMC, Technical Operations, or manufacturing is required.

Program/project management experience within pharmaceutical, biotechnology, or drug development environments is preferred.

Experience supporting analytical activities, formulation development, or related functions is also preferred.

Strong working knowledge of pharmaceutical development and CMC/Technical Operations activities across the product development lifecycle.

Working knowledge of core CMC disciplines, including Drug Substance/API Development, Analytical Development, Drug Product/Pharmaceutical Development, Manufacturing, Supply Chain, Quality, and CMC Regulatory.

Ability to integrate technical plans, milestones, dependencies, risks, and deliverables across multiple CMC disciplines, sub‑teams, and workstreams.

Understanding of upstream and downstream dependencies among CMC/Technical Operations activities and their potential impact on broader development program timelines and objectives.

Understanding of the interfaces among Technical Operations, Research, Clinical Development, Regulatory Affairs, Quality, Supply Chain, Finance, and other development functions.

Knowledge of CMC planning and readiness requirements associated with key development, manufacturing, clinical supply, and regulatory milestones.

Ability to partner effectively with technical and functional subject‑matter experts and translate complex technical strategies and activities into integrated program plans, milestones, risks, and execution priorities.

Ability to facilitate scenario planning and trade‑off discussions involving timelines, sequencing, resource constraints, technical dependencies, and execution priorities.

Understanding of program governance, risk management, decision management, and escalation practices within a pharmaceutical development and Technical Operations environment.

Familiarity with resource and capacity planning and the ability to provide leadership with meaningful visibility into workload, timing, dependencies, constraints, and program priorities.

Strong program and project management skills, with demonstrated ability to manage multiple complex programs, projects, or workstreams with competing priorities and deadlines.

Strong planning and organizational skills, with the ability to develop and maintain integrated plans, timelines, milestones, dependencies, critical paths, risks, and deliverables.

Strong cross‑functional collaboration and influencing skills, with the ability to build alignment, facilitate productive discussions, and drive execution in a matrixed environment.

Strong analytical, critical‑thinking, and problem‑solving skills, with the ability to evaluate complex information, identify risks and dependencies, develop options, and make sound recommendations.

Excellent written and verbal communication skills, with the ability to synthesize complex information and communicate program status, risks, decisions, and recommendations clearly to diverse audiences, including senior leaders.

Demonstrated ability to facilitate meetings, planning sessions, governance forums, scenario discussions, and decision‑making processes involving multiple functions and stakeholders.

Ability to operate with a high degree of independence within established objectives, exercising sound judgment regarding when to resolve issues directly and when escalation or broader leadership involvement is appropriate.

Strong understanding of risk, issue, dependency, and decision management practices and their application to complex development programs.

Ability to understand broader organizational objectives and downstream impacts and translate strategic or program objectives into actionable plans, priorities, and execution activities.

Strong continuous‑improvement mindset, with the ability to identify and recommend improvements to processes, workflows, governance, tools, reporting, and ways of working.

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.

The annual base salary we reasonably expect to pay is $130,800.00-$179,000.00.

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 30% 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.

We are a top place to work. Neurocrine Biosciences was named one of the FORTUNE Best Workplaces in Biopharma™ 2025. We were also named a Great Place to Work® Certified company.

OUR VALUES:

PASSION: We are driven and love what we do. We are committed to our goals and to making a difference.

INTEGRITY: We do the right thing for patients and our community. We take accountability. We speak up.

COLLABORATION: We trust one another. We are inclusive. We are respectful. We are transparent. Together we succeed.

INNOVATION: We seek and create optimal solutions.

TENACITY: We do not quit. We adapt. We accomplish what others cannot.

Come join our team during this exciting time of growth and opportunities!