b'nnnnnnnn Director, Global Supplier Quality Management - BioMarin Corporatennnn n n nnntntntntntntntntntntntntntntntntnnnnnnnnnnnnnnnnnnnnnn nn n n n n tttt n n n n n n n Companyn n n About Us n Leadership Team n Board of Directors n Responsibility n Giving n Patient Support n n n n n n Sciencen n n Our Science n Research & Development n Manufacturing n Clinical Trials n Publications n External Scientific Support n n n n n n Products & Pipelinen n n Overview n Products n Pipeline n Expanded Access n Medical Information n n n n n n Newsn n n Newsroom n Stories n Press Releases n Company Statements n n n n n n Careersn n n Careers at BioMarin n Fellowships n n n n n n Investorsn n n n n n n Locations n Contact n n n ttttttn n n n n Locations n Contact n n n n n n n n Searchn n n n tn tttttttttttttttn n n n n n n n n n tttttttn n n n n n ttn n n n n Search BioMarinn n n n n n n n nnn n n n n Back to Jobsn n n nn nn n n nn n n n n n United Statesn n n n n n n BioMarin Pharmaceuticaln nn n n Director, Global Supplier Quality Management n Location: United States n Workstyle: Remote Only n Apply n nn n Who We Are n BioMarin is a leading, global rare disease biotechnology company focused on delivering medicines for people living with genetically defined conditions. Founded in 1997, the San Rafael, California-based company has a proven track record of innovation, with multiple commercial therapies and a strong clinical and preclinical pipeline. Using a distinctive approach to drug discovery and development, BioMarin seeks to unleash the full potential of genetic science by pursuing category-defining medicines that have a profound impact on patients. n About Technical Operations n Our manufacturing and process development teams manage the production of our therapies for clinical trials and commercial markets. These engineers, technicians, scientists and support professionals continually provide quality assurance and ensure we meet all regulatory standards. We have manufacturing facilities in Northern California and in Shanbally, Ireland. Additionally, our supply chain teams procure the goods and services needed to support manufacturing and worldwide distribution. n SUMMARY DESCRIPTION n The Director, Global Supplier Quality Management is a senior leadership role with enterprise-wide authority and accountability for the governance, effectiveness, and continuous advancement of BioMarinxe2x80x99s global Supplier Quality Management framework across the external supply network for GMP/GDP materials. This role serves as the quality authority for suppliers and materials, ensuring sustained regulatory compliance, product quality, and patient safety while enabling uninterrupted and scalable business operations. xc2xa0 The Director defines and drives the global Supplier Quality vision and strategy and exercises decision-making authority across the full supplier lifecycle, in close partnership with Procurement and Technical Operations. This includes supplier qualification, raw material specification oversight, quality agreements, supplier changes, deviations, performance management, auditing, and inspection readiness. The role interfaces at the enterprise level with senior leaders across Quality, Technical Operations, Manufacturing, Legal and Procurement to prevent quality risk, improve supplier capability, and embed a consistent, risk-based approach across the global network. xc2xa0 As a key change leader within Quality, the Director is also accountable for advancing digital and data-enabled Supplier Quality capabilities, including the adoption of automation, advanced analytics, and artificial intelligence (AI). Through these capabilities, the role ensures proactive risk identification, data-driven decision-making, and scalable oversight aligned with BioMarinxe2x80x99s long-term business and quality strategy. This position requires deep GxP expertise, strong executive presence, and the ability to operate with authority and influence in a complex, global, matrixed organization. nn RESPONSIBILITIES: n Global Supplier Quality Strategy & Governance n n Establish and maintain a risk-based, fit-for-purpose Global Supplier Quality Management framework aligned with BioMarinxe2x80x99s Global Quality Management System (QMS) and global regulatory requirements. n Define and execute the global Supplier Quality strategy to ensure consistent oversight, compliance, inspection readiness, and continuous improvement across the external supply network. n Jointly with Procurement, hold end-to-end ownership of the Supplier Lifecycle Management program, spanning supplier selection, qualification, onboarding, performance management, change management, and lifecycle exit decisions. n Own and oversee Supplier Quality core processes, including supplier qualification and lifecycle management, quality agreements, supplier changes, deviations, CAPA, and supplier auditing activities related to external suppliers. n Develop and maintain governance models, metrics, and management review processes to monitor Supplier Quality performance and escalate compliance risks appropriately. n n Supplier Oversight, Risk Management & Performance Improvement n n Ensure quality oversight of external suppliers, with a primary focus on materials and services supporting Technical Operations. n Provide Quality oversight for raw material specification management, ensuring specifications are scientifically sound, compliant, and aligned with manufacturing and control strategies. n Develop, define, and apply risk-based supplier oversight and segmentation models to focus resources on critical suppliers and material risks. n Establish and manage key Supplier Quality performance indicators, ensuring trending, signal detection, and timely actions. n Lead supplier quality issue investigations, risk assessments, and mitigation strategies to prevent non-conformances from impacting BioMarin operations or patients. n Collaborate with Procurement and Suppliers to drive quality improvement initiatives and enhance supplier capability, robustness, and compliance. n n Auditing & Inspection Readiness n n Establish, manage, and continuously improve the global Supplier Auditing program for all GMP and GDP suppliers, including audit strategy, planning, execution, follow-up, and effectiveness verification. n Ensure supplier audit outcomes, identified risks, and corrective actions are appropriately evaluated, trended, and integrated into Supplier Lifecycle Management and Quality Management Review processes. n Support and represent Supplier Quality during regulatory inspections and external audits involving suppliers and the external supply network. n n Digital Transformation, Data & Artificial Intelligence n n Lead the digital advancement of Supplier Quality by defining and executing a Supplier Quality technology and data roadmap aligned with the broader Quality Digital Strategy. n Leverage advanced analytics, automation, and AI-enabled solutions to improve supplier performance monitoring, risk identification, trend analysis, audit effectiveness, and decision-making. n Drive effective use of Supplier Quality data by integrating information from QMS, ERP, and external systems to generate actionable insights across the supplier lifecycle. n Partner with IT, Quality Systems, and business stakeholders to implement sustainable, scalable digital and AI solutions that enhance Supplier Quality effectiveness and efficiency. n n Cross-Functional & Network Collaboration n n Partner closely with Global Procurement, Manufacturing, Technical Development and other key stakeholders to ensure supplier requirements are clearly defined, aligned with business needs, and embedded across the supplier lifecycle. n Collaborate with cross-functional teams to ensure documentation supporting sourcing decisions, supplier selection, raw material specifications, and material suitability is robust, compliant, and fit for purpose. n Represent Supplier Quality in cross-functional governance forums and during regulatory inspections and audits. n n Leadership, Talent & Organization Development n n Lead, coach, and develop a high-performing global Supplier Quality team across multiple geographies. n Establish clear roles, responsibilities, capabilities, and succession plans within the Supplier Quality organization. n Drive a consistent, standardized approach to Supplier Quality and supplier lifecycle governance across the global network while enabling flexibility where required. n Foster a culture of quality, continuous improvement, innovation, and accountability within the team. n Lead talent acquisition, onboarding, performance management, and career development initiatives. n n Financial & Business Management n n Develop, manage, and monitor budgets and long-range plans for the Global Supplier Quality function. n Ensure appropriate resourcing and capabilities are in place to meet growing business, compliance, supplier oversight, and digital transformation needs. n n EDUCATION: n n Bachelorxe2x80x99s degree in Life Sciences, Engineering, or a related discipline required. n Advanced degree (MS, PhD, MBA) desirable but not required. n Six Sigma or Lean certification desirable. n n EXPERIENCE: n n Minimum of 15 years of experience in Quality Assurance, Supplier Quality, Manufacturing, or related roles within a highly regulated industry (biotechnology, pharmaceutical, medical device, or combination products). n In-depth knowledge of global quality and regulatory requirements (e.g., GMP, GCP, GDP, ISO standards, 21 CFR). n Demonstrated experience leading global supplier quality programs and managing complex external supply networks. n Proven leadership experience with the ability to develop, mentor, and inspire high-performing teams. n Strong experience operating in a matrix, global environment and influencing without direct authority. n Experience leading or sponsoring transformational change, including digital transformation initiatives. n Demonstrated experience using data, analytics, and digital tools to improve quality outcomes; experience with AI-enabled solutions a strong plus. n Excellent communication, collaboration, and stakeholder management skills, including interaction with senior leadership and regulators. n n n WORKSTYLE: n n This role may be performed remotely.xc2xa0 However if you live within 100 miles of Novato, CA (zip 94903) the role reverts to hybrid requiring an onsite presence 2x each week n n 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. n 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. n n t The salary range for this position is: $176,000 to $242,000. BioMarin considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans. n nn Apply n n n n n n Recruitment Fraud Alert Notice n n n n 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. n 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. n 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. n For more information on how to recognize and report phishing scams visit: https://consumer.ftc.gov/articles/how-recognize-and-avoid-phishing-scams or https://consumer.ftc.gov/consumer-alerts/2023/01/looking-job-scammers-might-be-looking-you n n n n n Equal Opportunity Employer/Veterans/Disabled n 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. n If you have a disability and believe you need a reasonable accommodation in order to search for a job opening or apply for a position, emailxc2xa0Applicant_accommodations@bmrn.comxc2xa0with your request. nThis email address is not for general employment inquiries or correspondence. We will only respond to those requests that are related to the accessibility of the online application system due to a disability. n BioMarin Pharmaceutical does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. We handle all recruiting through our Talent Acquisition team xe2x80x93 please do not contact hiring managers directly. Agencies who wish to offer their services to BioMarin Pharmaceutical may contact us atxc2xa0talentacquisition@bmrn.com. nApplicants, please do not use this email address to submit resumes xe2x80x93 if you do so, you will be redirected to apply through the website. n Click here to review "EEO Is The Law" poster.xc2xa0Click here to review the Pay Transparency Nondiscrimination Statement.xc2xa0Click here to review the Notification of Employee Rights under Federal Labor Laws. n n nn nn nnn n n nt ttntt nttttttntttt ntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 250 milesnttttttWithin 500 milesnttttttWithin 1,000 milesnttttttWithin 2,000 milesnttttttWithin 5,000 milesntttttntttttntttttntttttntttt ttttntttntt ttnt n nnn nt nt ntt nttt ntttt Youxe2x80x99re leaving the BioMarin website. ntttt Links to sites outside of this website are provided as a resource to the viewer. 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