Manager, Global Supplier Performance & Metrics

Otsuka America Pharmaceutical Inc.; Carson City (NV); Remote; USD 108,000 - 161,000; Full time

Benefits offered by this job

Medical benefits

401(k) match

Tuition reimbursement

Paid holidays

Paid leave

Job summary

Otsuka America Pharmaceutical Inc. is seeking a Manager, Global Supplier Performance & Metrics to lead supplier quality oversight, KPI reporting, and risk management across external suppliers supporting global operations.

This remote, full-time position reports to the Senior Manager and collaborates with Global Quality, Regulatory, Supply Chain, and external partners. Key duties include serving as the quality representative for suppliers, developing dashboards, supporting audits, maintaining

Qualifications

• Bachelor’s degree in a scientific, engineering, or health-related discipline is required.
• Minimum of 3 years of progressive experience within the pharmaceutical, biotechnology, or medical device industry, with experience in Quality Assurance, Supplier Quality, External Manufacturing Quality, or CMO Management.
• Experience supporting supplier quality programs, supplier audits, quality systems, or external manufacturing operations is preferred.
• Experience using TrackWise Digital or comparable eQMS is required.
• Knowledge of FDA 21 CFR Parts 210, 211, and 11, EU GMP, EudraLex Volume 4, and ICH guidelines (Q7, Q9, Q10).
• Experience participating in supplier audits and supporting risk-based supplier management activities.

Responsibilities

• Serve as the primary Quality representative for assigned suppliers, including CMOs, CDMOs, laboratories, packaging suppliers, and other GMP service providers.
• Prepare and present supplier quality performance data in supplier governance meetings, Joint Steering Committees, and Business Review Meetings.
• Build collaborative relationships with supplier quality personnel to enable timely communication, issue resolution, and continuous improvement.
• Identify and escalate supplier quality concerns, performance risks, and compliance issues with recommended actions.
• Collect, maintain, and analyze Global Supplier Quality metrics and KPIs.
• Develop and maintain supplier performance dashboards and scorecards for routine business reviews.
• Prepare recurring supplier performance reports and trend analyses for management.
• Monitor supplier performance data for emerging risks and support mitigation activities.
• Support planning, coordination, and execution of supplier audits for API manufacturers, CMOs, packaging suppliers, and contract laboratories.
• Monitor CAPAs and ensure timely closure.
• Assist with drafting and maintaining supplier Quality Agreements.
• Support supplier qualification and ongoing risk assessment activities.
• Serve as a functional user of TrackWise Digital supplier quality modules and maintain supplier records.

Skills

Analytical thinking

Communication

Stakeholder collaboration

Organizational skills

QA/SQ/CMO experience

Education

Bachelor’s degree in science/engineering/health

3+ years pharmaceutical/biotech/medical device experience

Tools

TrackWise Digital

eQMS

Job description

Remote

Full time

R12736

Position Overview

Otsuka is seeking a motivated, detail-oriented, and analytical professional to serve as the Manager, Global Supplier Performance & Metrics. Reporting directly to the Senior Manager, Global Supplier Performance & Metrics, this role is responsible for supporting the execution of supplier quality management activities to ensure the quality, compliance, and performance of external suppliers supporting Otsuka's global operations.

The Manager is responsible for the day-to-day execution of supplier performance monitoring, supplier quality oversight, KPI reporting, audit support, and supplier risk management activities. Working collaboratively with Global Quality, Technical Operations, Supply Chain, Regulatory Affairs, and external suppliers, this position helps maintain a robust supplier quality framework aligned with global GMP, GDP, and applicable regulatory requirements.

1. Supplier Oversight & Operational Support

• Serve as the primary Quality representative for assigned suppliers, including CMOs, CDMOs, laboratories, packaging suppliers, and other GMP service providers.
• Participate in supplier governance meetings, Joint Steering Committees, and Business Review Meetings by preparing and presenting supplier quality performance data.
• Build collaborative working relationships with supplier quality personnel to facilitate timely communication, issue resolution, and continuous improvement.
• Identify and escalation supplier quality concerns, performance risks, and compliance issues to the Senior Manager with recommended actions.

2. Data Analytics, KPIs & Performance Reporting

• Collect, maintain, and analyze Global Supplier Quality metrics and key performance indicators.
• Develop and maintain supplier performance dashboards and scorecards supporting routine business reviews.
• Prepare recurring supplier performance reports, trend analyses, and management presentations.
• Monitor supplier performance data for emerging risks and support implementation of approved mitigation activities.

3. Supplier Qualification & Audit Support

• Support the planning, coordination, and execution of supplier audits for API manufacturers, drug product CMOs, packaging suppliers, and contract laboratories.
• Monitor supplier CAPAs and follow up to ensure timely closure.
• Assist with drafting, revising, and maintaining supplier Quality Agreements.
• Support supplier qualification and ongoing supplier risk assessment activities.

4. Quality Systems & Digital Tools

• Serve as a functional user of TrackWise Digital supplier quality modules, maintaining supplier profiles, audit records, deviations, CAPAs, and supplier performance documentation.
• Ensure supplier quality records remain accurate, complete, and inspection-ready.
• Identify opportunities to improve supplier quality processes, reporting, and system utilization.

Requirements & Qualifications

Education & Experience

• Bachelor's degree in a scientific, engineering, or health-related discipline (e.g., Chemistry, Biology, Pharmacy, Engineering) is required.
• Minimum of 3 years of progressive experience within the pharmaceutical, biotechnology, or medical device industry, with experience in Quality Assurance, Supplier Quality, External Manufacturing Quality, or CMO Management.
• Previous experience supporting supplier quality programs, supplier audits, quality systems, or external manufacturing operations is preferred.

Technical & Software Skills

• Experience using TrackWise Digital or comparable electronic Quality Management Systems (eQMS) is required.
• Working knowledge of FDA 21 CFR Parts 210, 211, and 11, EU GMP, EudraLex Volume 4, and applicable ICH guidelines (Q7, Q9, and Q10).
• Experience participating in supplier audits and supporting risk-based supplier management activities.

Soft Skills & Core Competencies

• Strong analytical ability with experience interpreting supplier quality metrics and identifying performance trends.
• Effective written and verbal communication skills with the ability to prepare clear reports and present findings to cross-functional teams.
• Demonstrated ability to build productive working relationships with internal stakeholders and external suppliers.
• Strong organizational skills and the ability to prioritize multiple assignments while supporting continuous improvement initiatives.

Competencies

Accountability for Results -

Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.

Strategic Thinking & Problem Solving -

Make decisions considering the long-term impact to customers, patients, employees, and the business.

Patient & Customer Centricity -

Maintain an ongoing focus on the needs of our customers and/or key stakeholders.

Impactful Communication -

Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.

Respectful Collaboration -

Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.

Empowered Development -

Play an active role in professional development as a business imperative.

Minimum $107,718.00 - Maximum $161,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

Application Deadline

This will be posted for a minimum of 5 business days.

Company Benefits

Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.

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Disclaimer

This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting [e-mail] .