Director — Global Supply Chain End-to-End Process Capabilities

BioMarin Pharmaceutical Inc.

San Rafael (CA)

On-site

USD 180,000 - 280,000

Full time

14 days+
Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Benefits offered by this job

Health insurance
401(k) plan

Job summary

BioMarin Pharmaceutical Inc. is seeking a Director, Supply Chain Framework to design, standardize, and govern end-to-end supply chain processes on a global scale. This leader will drive process transformation, ensure operational consistency, and promote cross-market adoption across Supply Chain, Manufacturing, Clinical, and Commercial.

You will embed best practices, deliver sustained improvements, and build a high-performing team with strong governance and stakeholder collaboration.

Qualifications

  • Experience leading enterprise transformation or global process ownership.
  • 12+ years of experience with global supply chain processes.
  • Knowledge of S&OP/IBP, planning, logistics, Product Management.
  • Certification in Lean or Six Sigma is desirable.

Responsibilities

  • Design and govern end-to-end supply chain processes with global scope.
  • Lead transformation and optimization initiatives to improve efficiency and agility.
  • Partner with Digital/Analytics to embed data-driven solutions.
  • Build capability with training and change management programs.
  • Represent Supply Chain Excellence in senior forums and governance bodies.

Skills

Enterprise transformation
Global process ownership
S&OP/IBP
Governance
Stakeholder management
Lean Six Sigma

Education

Bachelor's in Supply Chain/Engineering/Business

Job description

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.

Role Overview

The Director, Supply Chain Framework, will lead the design, standardization, and governance of BioMarin’s end-to-end supply chain processes. This leader drives process transformation, operational consistency, and cross-market adoption while partnering across Supply Chain, Manufacturing, Clinical, and Commercial to embed best practices and deliver sustained performance improvement.

Key Responsibilities
Process Design & Governance
  • Partner with the Global Supply Chain Leadership team to develop and maintain end-to-end process standards across Planning, Distribution, Launches, Variations, Value Chain, and Clinical Supply Chain that drive consistency, scalability, and alignment with corporate standards.
  • Manage changes to these processes through clearly defined approval gates and compliance checks, aligned with global design principles and applicable GxP/regulatory requirements.
  • Build and sustain the frameworks, documentation, and governance routines that keep processes auditable, transparent, and audit-ready.
  • Serve as the global process authority for end-to-end supply chain process, with accountability for decision governance, prioritization, and escalation across functions and regions.
Transformation & Optimization
  • Lead the Supply Chain end-to-end process redesign initiatives aimed at improving efficiency, quality, and agility throughout the supply chain in its current scope.
  • Partner with Digital and Analytics teams to integrate advanced technologies and data-driven solutions into core processes for Supply Chain scope.
  • Continuously identify bottlenecks and implement structured improvement plans that deliver measurable business impact.
Adoption & Capability Building
  • Drive implementation of new processes, ensuring seamless integration across all supply chain functions.
  • Design and deliver capability-building programs, including training and change management strategies, to foster adoption.
  • Monitor adherence and performance, using insights to refine processes and sustain long‑term improvements.
Cross-Functional Leadership
  • Build, lead, and develop a high-performing team, including direct and dotted-line reports, responsible for process excellence, governance, capability building, and continuous improvement.
  • Align process strategies with broader business objectives by collaborating with Manufacturing, Clinical, QA, Commercial, and Finance.
  • Serve as a process owner and escalation point for critical issues, ensuring timely resolution and stakeholder alignment.
  • Represent Supply Chain Excellence in senior leadership forums, steering committees, and governance bodies to drive alignment, investment decisions, and adoption.
Performance & Reporting
  • Deliver measurable improvements in supply reliability, inventory efficiency, launch execution, compliance readiness, and end-to-end planning effectiveness.
  • Establish KPIs, dashboards, and reporting mechanisms to measure process performance and maturity across the organization.
  • Conduct regular assessments to identify improvement opportunities and benchmark against industry best practices.
Required Qualifications
  • Experience leading enterprise transformation or global process ownership.
  • Bachelor’s degree in Supply Chain, Engineering, Business or related field; MBA or master’s preferred.
  • 12+ years of experience with global supply chain processes.
  • Knowledge of S&OP/IBP, planning, logistics, Product Management.
  • Demonstrated success driving cross-functional transformation.
  • Strong governance, influence, and stakeholder management skills across global, matrixed organization.
  • Certification in Lean, Six Sigma Black Belt, or other recognized Operational Excellence methodology is highly desirable.

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, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Ireland Safety Responsibility

Support the organisation’s commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.

Ireland Safety Responsibility

Support the organisation’s commitment to environmental protection, injury prevention, and continual improvement of EHS management systems. Actively contribute to a safe and environmentally responsible workplace by identifying hazards, reporting incidents and participating in EHS initiatives and training.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Director — Global Supply Chain End-to-End Process Capabilities
Director — Global Supply Chain End-to-End Process Capabilities

biomarin • San Rafael (CA)

On-site
USD 180,000 - 240,000
Director — Global Supply Chain End-to-End Process Capabilities
Director — Global Supply Chain End-to-End Process Capabilities

BioSpace • San Rafael (CA)

On-site
USD 180,000 - 260,000
Associate Director and Business Process Manager, Distribution, Supply, and Network Planning
Associate Director and Business Process Manager, Distribution, Supply, and Network Planning

Initial Therapeutics, Inc. • San Rafael (CA)

On-site
USD 120,000 - 160,000
Senior Manager, External QA Validation
Senior Manager, External QA Validation

BioSpace • Novato (CA)

On-site
USD 150,000 - 210,000
Director, Head of Performance Management, Advanced Analytics and Reporting
Director, Head of Performance Management, Advanced Analytics and Reporting

biomarin • United States

On-site
USD 180,000 - 280,000
Senior Scientist 2, Chemical Development & Manufacturing
Senior Scientist 2, Chemical Development & Manufacturing

biomarin • Novato (CA)

Hybrid
USD 150,000 - 190,000
Senior Scientist 2, Chemical Development & Manufacturing
Senior Scientist 2, Chemical Development & Manufacturing

BioMarin Pharmaceutical Inc. • Novato (CA)

On-site
USD 110,000 - 170,000
Manager, Global E2E Product Supply Planning
Manager, Global E2E Product Supply Planning

biomarin • San Rafael (CA)

Hybrid
USD 110,000 - 150,000
Associate Director, Product Artwork Management
Associate Director, Product Artwork Management

biomarin • United States

On-site
USD 180,000 - 270,000
Senior Manager, External QA Validation
Senior Manager, External QA Validation

BioMarin Pharmaceutical Inc. • Novato (CA)

On-site
USD 170,000 - 210,000