BioMarin Pharmaceutical

Sr. Technical Manager, Supplier Quality Management BPO

BioMarin Pharmaceutical$120K — $150K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Engineering, or related field required; advanced degree (MS, PhD, MBA) preferred.
  • Minimum of 10 years in Quality Assurance, Supplier Quality, or related roles in regulated industries.
  • Strong knowledge of global quality and regulatory standards (GMP, GDP, ISO, 21 CFR).
  • Experience managing supplier audit programs for GMP/GDP materials is essential.
  • Proven ability to define and manage KPIs with a focus on continuous improvement.
  • Hands-on experience with digital, automation, and AI solutions in quality settings is strongly preferred.
  • Excellent organizational and stakeholder management skills for effective communication.

Responsibilities

  • Manage the execution of the GMP/GDP material supplier audit program, ensuring timely completion and compliance.
  • Serve as Business Process Owner for SQM processes, driving consistency across the global supplier base.
  • Define and maintain performance metrics for Supplier Quality, fostering a data-driven culture.
  • Lead the digitalization and AI implementation roadmap for Supplier Quality processes and tools.
  • Support Supplier Quality Category Manager activities, ensuring quality agreements and risk assessments are completed.
  • Collaborate with cross-functional teams to enhance supplier quality management and resolve issues.
  • Provide mentorship to the Supplier Quality team, promoting continuous improvement and collaboration.

Benefits

  • Opportunities for professional development and further education support.
  • Collaborative and innovative company culture.
  • Access to cutting-edge technology and tools in Supplier Quality management.
  • Participation in a global network of quality professionals.
Full Job Description
Description

SUMMARY DESCRIPTION

The Sr. Manager, QA, Supplier Quality Management BPO is an operational leadership role responsible for the execution, day-to-day management, and continuous improvement of core Supplier Quality Management (SQM) processes supporting BioMarin's external supply network for GMP/GDP materials. This role serves as the Business Process Owner (BPO) for the SQM quality process and is accountable for ensuring the processes are consistently applied, effectively monitored, and continuously enhanced across the global supplier base.

The Sr. Manager owns and executes the GMP/GDP material audit program, tracks and maintains key performance metrics for the Supplier Quality department and drives measurable continuous improvement initiatives. Additionally, this role leads the digitalization and AI enablement agenda for the department - translating strategic direction from the Director into practical implementation of automation, analytics, and AI-enabled tools that improve efficiency, oversight, compliance and decision-making.

The Sr. Manager also provides hands-on support to the execution of Supplier Quality Category Manager activities, partnering closely with category managers, Procurement, and Technical Operations to ensure supplier qualification, quality agreements, changes, deviations, and performance activities are executed on time and to standard.

This position requires strong GxP execution expertise, disciplined process management, and the ability to operate effectively in a matrixed, cross-functional environment with a focus on delivery, compliance, and operational excellence.

RESPONSIBILITIES

GMP/GDP Material Audit Program Management
  • Manage the end-to-end execution of the GMP/GDP material supplier audit program (outsourced), including annual audit planning, scheduling, execution oversight, follow-up, CAPA tracking, and effectiveness verification.
  • Ensure audits are completed on schedule in alignment with the approved audit plan.
  • Coordinate internal and third-party auditors, ensuring consistent audit standards, timely reporting, and closure of audit observations.
  • Ensure supplier audit outcomes, identified risks, and corrective actions are appropriately documented, trended, and integrated into Supplier Lifecycle Management and Quality Management Review processes.
  • Support and represent Supplier Quality during regulatory inspections and external audits involving suppliers, providing audit program data and evidence of effectiveness.

Business Process Owner (BPO) - Supplier Quality Management Processes
  • Serve as the Business Process Owner for the Supplier Quality Management quality processes, including supplier qualification and lifecycle management, quality agreements, supplier changes, supplier deviations/CAPA, and supplier auditing.
  • Proactively monitor and maintain the health of these processes and their subprocesses, ensuring consistency of application across the global supplier base.
  • Maintain and update associated procedures, work instructions, templates, and training materials to sustain compliance with current and evolving global health authority requirements.
  • Drive process standardization, harmonization, and simplification across sites and functions.
  • Partner with Quality Systems, Compliance, and IT to ensure supporting systems and workflows enable efficient and compliant process execution.

Performance Metrics & Continuous Improvement
  • Define, track, and maintain the key performance indicators (KPIs) and metrics for the Supplier Quality department, including supplier performance, process health, audit program execution, and issue resolution timeliness.
  • Establish and manage reporting cadences and dashboards to enable trending, signal detection, and timely management review.
  • Identify improvement opportunities from metric trends and lead cross-functional continuous improvement initiatives to address them.
  • Drive a culture of data-driven decision-making and operational excellence within the Supplier Quality team.
  • Support management review processes with accurate, actionable performance data.

Digitalization & AI Implementation
  • Lead the execution of the department's digitalization and AI implementation roadmap, in alignment with the broader Quality Digital Strategy defined by the Director.
  • Identify, evaluate, and implement automation, advanced analytics, and AI-enabled solutions to improve supplier performance monitoring, risk identification, trend analysis, audit effectiveness, and process efficiency.
  • Partner with IT, Quality Systems, and business stakeholders to deliver sustainable, scalable digital solutions, including requirements definition, system configuration, and change management.
  • Drive effective use of Supplier Quality data by integrating information from eQMS, ERP, and external systems to generate actionable insights.
  • Champion adoption of digital and AI tools within the Supplier Quality team through training, communication, and hands-on support.

Supplier Quality Category Manager Execution Support
  • Support the execution of Supplier Quality Category Manager activities across assigned material categories, ensuring timely completion of supplier qualification, onboarding, and lifecycle management tasks.
  • Assist in the development and maintenance of Quality Technical Agreements with global suppliers to define quality expectations and responsibilities.
  • Support risk-based approaches to identify, assess, and mitigate supplier-related risks, ensuring continuity of supply and material quality.
  • Provide execution support for supplier performance management (scorecards), supplier investigations, CAPAs, and change assessments as needed.
  • Collaborate with category managers, Procurement, Manufacturing, and site QA to resolve supplier quality issues and drive supplier performance improvement.

Cross-Functional Collaboration
  • Partner with Global Procurement, Manufacturing, Technical Development, site QA, and other stakeholders to ensure supplier quality requirements are executed effectively across the supplier lifecycle.
  • Represent Supplier Quality in cross-functional process forums, working groups, and improvement projects.
  • Promote knowledge sharing and consistent application of best practices across sites and functions.

People & Team Contribution
  • Provide day-to-day guidance, coaching, and technical mentorship to Supplier Quality team members supporting the audit program, BPO activities, metrics, and digital initiatives.
  • Support onboarding, training, and capability development within the Supplier Quality team.
  • Foster a culture of quality, accountability, collaboration, and continuous improvement.

EDUCATION
  • Bachelor's degree in Life Sciences, Engineering, or a related discipline required.
  • Advanced degree (MS, PhD, MBA) desirable but not required.
  • Six Sigma, Lean, or auditor certification (e.g., ASQ CQA) desirable.


EXPERIENCE
  • Minimum of 10 years of experience in Quality Assurance, Supplier Quality, Manufacturing, or related roles within a highly regulated industry (biotechnology, pharmaceutical, medical device, or combination products).
  • Solid working knowledge of global quality and regulatory requirements (e.g., GMP, GDP, ISO standards, 21 CFR).
  • Demonstrated experience executing and managing supplier audit programs for GMP/GDP materials.
  • Prior experience as a Business Process Owner or equivalent process ownership role within a QMS environment strongly preferred.
  • Proven track record of defining and managing KPIs and delivering measurable continuous improvement outcomes.
  • Hands-on experience implementing digital, automation, analytics, or AI-enabled solutions in a Quality or regulated environment strongly preferred.
  • Experience working in a matrixed, global environment and driving results through influence as well as direct execution.
  • Excellent communication, collaboration, and stakeholder management skills, including the ability to present data and defend approaches to senior management and inspectors.
  • Strong organizational skills with the ability to manage multiple priorities and deliver on time.


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.

About BioMarin Pharmaceutical

BioMarin Pharmaceutical Inc. is a biotechnology company that develops and commercializes innovative therapies for patients with serious and life-threatening rare and ultra-rare genetic diseases. The company's portfolio consists of seven commercialized products and multiple clinical and pre-clinical product candidates. BioMarin's products are used to treat patients suffering from rare genetic diseases such as phenylketonuria, achondroplasia, and Batten disease. The company was founded in 1997 and is headquartered in San Rafael, California.
Learn more about BioMarin Pharmaceutical
Size
3,045 employees
Market Cap
$19.2 billion
Industry
Net Income
$859.1 million
Founded
2003
5 Year Trend
+10.6%
Revenue
$1.8 billion
NASDAQ

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