Senior Director, Integrated Planning & Analytics - Global Supply Chain

Posted 6 Days Ago
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Cork, IRL
In-Office
Senior level
Biotech • Pharmaceutical • Manufacturing
The Role
Leads global Integrated Business Planning across demand, supply, inventory, capacity, and financial objectives for a rare disease supply network. Owns IBP and S&OE governance, long-range capacity modeling, inventory strategy, scenario planning, analytics, and planning technology vision. Partners with commercial, clinical, manufacturing, quality, regulatory, medical, finance, and IT stakeholders while developing planning teams, driving organizational change, and ensuring resilient, patient-centered supply continuity.
Summary Generated by Built In

Who We Are
BioMarin is a leading rare disease biotechnology company focused on genetically defined conditions.
Guided by our purpose to develop medicines that make a profound impact on people’s lives, our global teams have delivered a portfolio of therapies since our founding in 1997. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. More recently, with the close of the Amicus acquisition, our portfolio has expanded to include therapies for Fabry disease and Pompe disease, expanding our ability to reach more people living with rare genetic conditions.
Our success comes from our unwavering commitment to excellence, our deep understanding of patient needs, our scientific expertise, and our world-class manufacturing capabilities. At the heart of BioMarin is a dedicated team of the brightest minds in the industry working together to deliver innovative therapies to patients and families around the world.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

Senior Director, Integrated Planning & Analytics - Global Supply Chain

Location: Shanbally, Ringaskiddy, Cork ( hybrid role 2 days per week onsite)

Closing date: Friday 15th August 2026

Role Summary


The Senior Director, Integrated Planning & Analytics, leads enterprise planning across demand, supply, inventory, capacity, and financial objectives through Integrated Business Planning (IBP). This role drives profitable growth, operational agility, and patient-centric outcomes across a global rare disease supply network by connecting decisions across Commercial, Clinical, Manufacturing, Quality, Regulatory, Medical Affairs, and Finance.

In a dynamic portfolio shaped by new indications, label expansions, named-patient and compassionate use programs, and clinical-to-commercial transitions, this leader strengthens supply resilience, manages risk, and builds planning capabilities for long-term growth.

As the global process owner for IBP, you will lead forward-looking decision-making across a 24–60-month horizon, including long-range capacity planning and modelling, inventory strategy, and data analytics that support reliable supply and patient access.

Key Responsibilities

1. IBP Process Ownership in a Rare Disease Environment

  • Own the global IBP framework for rare disease planning, addressing demand variability, small batches, long lead times, and constrained capacity.
  • Establish and maintain a consistent IBP cadence (Product Review, Demand Review, Supply Review, Integrated Reconciliation, Executive IBP).
  • Own the S&OE (Sales & Operations Execution) process, ensuring near-term demand, supply, and inventory decisions are aligned to the broader IBP framework and escalated appropriately.
  • Embed patient-centric planning principles into the IBP cycle (e.g., emergency orders, compassionate use, urgent clinical supply requests).
  • Ensure seamless integration of clinical and commercial planning due to overlapping supply sources and shared manufacturing assets.

2. Rare Disease Demand, Supply & Inventory Integration

  • Oversee reconciliation of commercial, patient, named-patient, early-access, and clinical trial demand signals.
  • Ensure supply plans reflect long cycle times, yield variability, cold-chain requirements, and CMO dependencies.
  • Lead Inventory Management to define inventory policies, targets, and positioning strategies that minimize expiry while guaranteeing immediate patient access for ultra-low-volume therapies.
  • Lead risk-based scenario planning for demand surges (e.g., new diagnoses, outbreaks, compassionate use clusters), supply disruptions, or single-source component issues.

3. Cross-Functional Leadership  &  Governance

  • Chair IBP forums across Commercial, Clinical Operations, Technical Operations, Manufacturing, Quality, Regulatory, Finance, and Medical.
  • Establish governance and decision rights for trade-offs such as allocation priorities, safety stock strategies, and launch readiness.
  • Lead structured decision-making in Executive IBP, ensuring senior leaders have clear scenarios, risks, and recommendations.
  • Drive alignment across global, regional, and country planning, accounting for reimbursement and access variability.

4. People Leadership: 

  • Lead the team of Integrating Planning & Analytics professionals, through strong development and mentoring while creating a culture of high accountability and innovation.   
  • Ensure there are departmental performance goals and objectives that the team of integrated planners can leverage to develop their respective objectives and provide performance feedback related to business objectives.
  • Create a training curriculum to support Integrated Planning & Analytics Team’s development responsibilities.
  • Influence teams across the supply chain planning organization to improve their maturity and collaboration through a harmonized integrated planning playbook maximizing optimal support to the planning cycles.

5. Financial & Portfolio Integration

  • Partner closely with Finance, particularly during AOP/LRP cycles, to embed operational, revenue, COGS, and margin considerations into IBP.
  • Integrate portfolio plans including new indications, lifecycle extensions, label expansions, and transitions from clinical supply platforms to scaled commercial supply.
  • Support business case development for strategic investments (redundant capacity, alternate sites, new technology platforms) and lead long-range capacity planning/modelling to ensure the network can support future portfolio growth, new indications, and evolving patient demand.

6. Data, Systems & Analytics

  • Leading and enhancing performance management and visualization efforts, specifically improving dashboards that can be used across markets, supply, finance, and overall performance management  
  • Define the IBP technology vision with Digital/IT, including platforms for complex, low-volume, high-variability planning.
  • Ensure data quality for critical demand, therapy, batch, expiry, and distribution attributes.
  • Lead Data Analytics to develop advanced planning insights, improve forecast ability of ultra-small populations, and evaluate risk-based scenarios for proactive decision-making.

7. Stakeholder Engagement & Change Leadership

  • Drive adoption of IBP behaviours in a highly cross-functional, mission-driven rare disease culture.
  • Communicate clearly with senior leadership on risks, trade-offs, and opportunities, always emphasizing patient impact.
  • Build planning capability across global and regional teams and mentor planners supporting rare disease products.
  • Function as an internal expert and thought leader on best-practice IBP/S&OP for rare disease and biologics.

KPIs & Metrics: This role will influence:

  • Patient & Service Metrics
  • Supply Reliability Metrics
  • Inventory & Waste Metrics
  • Forecast & Financial Metrics
  • IBP Process Health Metrics

Qualifications

Required:

  • Bachelor’s degree in Supply Chain, Engineering, Business, Life Sciences, or related field.
  • 12+ years of progressive supply chain or operations leadership in biotech, pharmaceutical, or rare disease environments.
  • Proven leadership of global S&OP/IBP processes, including long-range capacity planning, inventory strategy, and executive decision support.
  • Strong command of ERP, advanced planning systems, and analytics tools that support scenario modelling and business decisions.
  • Demonstrated success leading through senior executives in complex, matrixed global organizations.
  • Deep understanding of life science supply chains, including access variability, long lead times, biologics complexity, and patient-critical supply continuity.
  • Strong financial acumen with proven cross-functional leadership in matrixed organizations.

Preferred:

  • Master’s degree (MBA, MS, or equivalent).
  • Experience with biologics, gene therapy, enzyme replacement therapies, or other complex rare disease modalities.
  • APICS/ASCM, SCOR-P, or equivalent certification.
  • Experience integrating clinical and commercial supply processes.
  • Familiarity with global regulatory / GxP constraints uniquely impacting rare disease therapies.

Core Competencies

  • Patient-Centric Mindset — prioritizes therapy availability for individuals with life-altering conditions.
  • Strategic Systems Thinking — understands complex network interactions across clinical and commercial supply, including long-range capacity and inventory trade-offs.
  • Executive Influence — builds alignment, shapes decisions, and leads cross-functional forums with credibility in complex matrix environments.
  • Data Analytics & Financial Acumen — translates operational scenarios into financial and patient impacts using data-driven insights and advanced planning analytics.
  • Inventory Strategy — balances service, waste, and working capital through thoughtful inventory policy, positioning, and risk management.
  • Risk Management — proactive identification and mitigation of rare disease supply vulnerabilities.
  • Change Leadership — able to embed new planning behaviours, tools, and processes in a global organization.

Travel Requirements

  • International travel (10–25%) to manufacturing sites, affiliates, clinical hubs, and global planning workshops.

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Skills Required

  • Bachelor's degree in Supply Chain, Engineering, Business, Life Sciences, or a related field
  • 12+ years of progressive supply chain or operations leadership experience in biotech, pharmaceutical, or rare disease environments
  • Experience leading global S&OP or IBP processes, including long-range capacity planning, inventory strategy, and executive decision support
  • Strong command of ERP, advanced planning systems, and analytics tools supporting scenario modeling and business decisions
  • Demonstrated success leading through senior executives in complex, matrixed global organizations
  • Deep understanding of life science supply chains, including access variability, long lead times, biologics complexity, and patient-critical supply continuity
  • Strong financial acumen and proven cross-functional leadership in matrixed organizations
  • Master's degree, MBA, MS, or equivalent
  • Experience with biologics, gene therapy, enzyme replacement therapies, or other complex rare disease modalities
  • APICS, ASCM, SCOR-P, or equivalent certification
  • Experience integrating clinical and commercial supply processes
  • Familiarity with global regulatory or GxP constraints affecting rare disease therapies

BioMarin Pharmaceutical Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about BioMarin Pharmaceutical Inc. and has not been reviewed or approved by BioMarin Pharmaceutical Inc..

  • Healthcare Strength Benefits are often characterized as comprehensive, spanning medical, dental, vision, life and disability coverage, along with FSAs/HSAs and an EAP. Feedback suggests these health offerings are consistently regarded as strong and at times "industry best".
  • Leave & Time Off Breadth Leave and time off are described as generous, with structured vacation progression, dedicated sick time, and a company-observed winter break among many holidays. Feedback suggests this breadth of paid time away is a standout element of the total rewards.
  • Retirement Support Retirement support is underpinned by a 401(k) savings plan with a company match. Feedback suggests these retirement programs contribute meaningfully to overall compensation value.

BioMarin Pharmaceutical Inc. Insights

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The Company
HQ: San Rafael, CA
3,270 Employees
Year Founded: 1997

What We Do

Founded in 1997, BioMarin is a global biotechnology company dedicated to transforming lives through genetic discovery. The company develops and commercializes targeted therapies that address the root cause of the genetic conditions that it seeks to treat, helping to better the lives of those struggling with rare genetic disease. BioMarin discoveries have led to eight first or best-in-class commercial treatments and a pipeline of multiple product candidates applying the same science-driven, patient-forward approach to broader group of genetic disorders. The more innovative solutions developed, the more lives BioMarin can impact. Recruitment Fraud Alert Notice Please be aware of fraud or scams from individuals, organizations and/or internet sites claiming to represent BioMarin in recruitment activities. We have an established recruitment process which is required for all posted positions by BioMarin prior to issuing an offer of employment. This BioMarin process requires formal interviews conducted live with personnel representing BioMarin and never requires payments or fees from job applicants. BioMarin does not conduct interviews via texting tools such as RingCentral. In the event you receive a suspicious email message about recruiting on behalf of BioMarin, unless it’s from a BioMarin authorized recruiting partner, do not provide any personal information or pay any fees. Qualified and interested candidates should apply to current openings directly through this BioMarin website. BioMarin accepts no responsibility for any costs or charges incurred as a result of fraudulent activity. If you have lost money or provided your personal identifying information, please contact your bank and report the matter to the FBI via www.ic3.gov. We would also suggest you notify your local police department and monitor your credit. We appreciate your interest in BioMarin & encourage you to visit http://careers.biomarin.com/career-areas to review job opportunities.

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