biomarin
biomarin17d ago
New

Sr Category Manager, Contract Manufacturing, GSP

United StatesUnited StatesRemotesenior
Category ManagerProcurement & Purchasing
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Quick Summary

Overview

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,

Technical Tools
Category ManagerProcurement & Purchasing

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.

Requirements

~2 min read
  •  5+ years of progressive experience in sourcing, procurement, or category management, preferably within biotech or pharmaceutical manufacturing
  • Experience supporting or leading sourcing for external manufacturing services (CDMOs/CMOs), with exposure to Drug Substance, Drug Product, or Packaging
  • Understanding of pharmaceutical manufacturing processes and supply chains, including biologics and/or small molecule production
  • Demonstrated experience executing sourcing events, supplier selection, and contract negotiations
  • Working knowledge of GxP environments and regulatory frameworks (FDA, EMA, ICH)
  • Proven ability to deliver cost savings and value beyond price (e.g., service, flexibility, risk mitigation)
  • Experience collaborating in cross-functional, matrixed environments
  • Strong analytical skills, including spend analysis, cost modeling, and supplier evaluation
Success and Leadership Competencies
  • Execution focus: Ability to independently manage sourcing initiatives from strategy through implementation
  • Business partnership: Effectively collaborate with technical and operational stakeholders to align sourcing with business needs
  • Commercial acumen: Skilled in negotiations, cost analysis, and contract structuring
  • Supplier management: Build productive, performance-driven relationships with CDMOs
  • Problem solving: Navigate supply and supplier challenges with practical, solutions-oriented approaches
  • Communication: Clearly articulate sourcing recommendations and trade-offs to stakeholders
Education and Technical Skills
  • Bachelor’s degree in engineering, Supply Chain Management, Business Administration, Life Sciences, Engineering, or related field required;
  • MBA or advanced degree (MS, PhD) in relevant preferred.
  • Technical experience in pharmaceutical manufacturing processes for both small molecules and biologics preferred. Including familiarity with cGMP requirements, regulatory frameworks (FDA, EMA, ICH), quality systems (ISO standards), and pharmaceutical supply chain complexity.
  • Proficiency in strategic sourcing methodologies, category management frameworks, supplier relationship management (SRM) systems, and spend analysis tools is required.
  • Experience with contract lifecycle management, e-sourcing platforms, and procurement analytics is essential.
  • Strong project management capabilities with ability to manage multiple complex sourcing initiatives simultaneously while meeting aggressive timelines.
  • Excellent written and verbal communication skills with ability to present complex sourcing strategies and recommendations to executive audiences.
  • Experience working in global, matrixed organizations with proven ability to influence without direct authority.


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.

Responsibilities

~1 min read
Conduct rigorous CDMO selection due diligence covering technical capabilities, regulatory compliance, quality systems, IP ownership structures, and capacity planning. Evaluate CDMO partners on specialized capabilities including biologics manufacturing, sterile injectables, and advanced modalities, ensuring alignment with BioMarin's pipeline requirements and key partner organizations within BioMarin including Global External Operations and External Quality.
Lead contract negotiations with CDMO/CMO partners, establishing commercial terms, Service Level Agreements (SLAs), technology transfer protocols, and IP protections. Structure risk-adjusted governance frameworks that protect BioMarin's interests while enabling collaborative partnerships.
Partner closely with External Manufacturing, Quality, Supply Chain, Technical Development Services, and Regulatory teams to ensure category strategies align with technical requirements, regulatory standards, and business objectives. Bridge the gap between strategic sourcing and operational reality, ensuring identified savings reach the bottom line.
Build diversified and resilient supplier networks that mitigate geopolitical risks, capacity constraints, and supply disruptions. Implement dual-sourcing strategies, strategic inventory buffers, and supply chain regionalization to reduce single-market dependencies while maintaining lean operations [7].
Maintain deep market knowledge of the CDMO landscape, including emerging technologies, capacity availability, pricing trends, and competitive dynamics. Monitor regulatory changes, sustainability requirements (especially Scope 3 emissions), and compliance demands to ensure procurement strategies remain ahead of industry shifts [8].
Present sourcing strategies, supplier performance metrics, cost savings achievements, and risk assessments to executive leadership. Serve as the strategic thought-partner for BioMarin's Global External Operations and Network Strategy organizations.

Location & Eligibility

Where is the job
United States
Remote within one country
Who can apply
Open to applicants worldwide

Listing Details

Posted
May 20, 2026
First seen
June 6, 2026
Last seen
June 6, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
27%
Scored at
June 6, 2026

Signal breakdown

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biomarinSr Category Manager, Contract Manufacturing, GSP