R&D Supplier Quality Manager

Amgen Inc.; United States; Remote; USD 104,000 - 141,000; Full time

Benefits offered by this job

Comprehensive benefits package

Stock-based incentives

Flexible work options

Career development opportunities

Job summary

Amgen in the United States is seeking a highly motivated R&D Supplier Quality Manager to support qualification, oversight, and continuous improvement of suppliers contributing to Amgen’s R&D pipeline and mission to serve patients.

You will lead risk-based supplier assessments, audits, and lifecycle management across GxP systems, ensuring data integrity, security, and regulatory compliance, with travel up to 10%.

Qualifications

• Doctorate or advanced degree in Life Sciences, Engineering, or related field.
• Strong knowledge of GxP, ISO standards and regulatory expectations.
• Experience with supplier quality risk assessment and audits.
• Experience with AI-enabled GxP systems preferred.
• Ability to work in cross-functional teams and in a matrixed environment.

Responsibilities

• Conduct risk-based supplier assessments, qualification, audit and lifecycle management with quality agreements.
• Lead or support risk-based qualification and oversight of suppliers using GxP computerized systems.
• Assess supplier AI-enabled GxP systems to ensure data integrity, security, and controls.
• Plan, lead, and document risk-based audits of supplier GxP systems and processes.
• Review supplier quality systems for lifecycle management including validation and change control.
• Monitor supplier performance, KPIs, and drive CAPA closure and governance.

Skills

Quality management

GxP

Audits

Data integrity

Regulatory knowledge

Cross-functional collaboration

Risk assessment

Education

Doctorate

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma

Tools

Veeva

TrackWise

GxP software tools

Job description

Career Category: Quality

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award‑winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

R&D Supplier Quality Manager

What you will do

Let’s do this. Let’s change the world. Amgen is seeking a highly motivated R&D Supplier Quality Manager to support the qualifications, oversight, and continuous improvement of suppliers that contribute to Amgen’s R&D pipeline and our mission to serve patients.

Key Responsibilities

• Conduct risk-based supplier assessments, qualification, audit and lifecycle management, including quality agreements across various R&D service categories.
• Lead or support risk-based qualification and ongoing oversight of suppliers that utilize and/or provide GxP computerized systems, interfaces and devices to support clinical and preclinical activities.
• Assessment and oversight of supplier AI-Enabled GXP computerized systems used to support clinical and preclinical activities ensuring compliance to defined procedural controls, policies and standards .
• Plan, lead, and document risk-based audits of supplier GxP computerized systems and associated quality processes to assess regulatory compliance, validation and lifecycle controls, data integrity, security, and the effectiveness of corrective and preventive actions.
• Assess supplier quality systems and controls for computerized system lifecycle management, including validation, data integrity, security, access management, change and configuration management, incident and problem management, backup, recovery, business continuity, and decommissioning.
• Review risk-appropriate quality and technical requirements in supplier contracts and quality agreements, including validation documentation, audit trails, electronic records and signatures, subcontractor controls, regulatory inspection support, data ownership, data retention, and notification of significant changes or incidents.
• Participate in supplier governance and periodic reviews; evaluate service performance, validation status, changes, deviations, incidents, audit outcomes, emerging risks, and CAPA effectiveness, and elevate GxP or data integrity concerns.
• Support inspection readiness and regulatory responses related to supplier’s computerized systems; partner with system owners and subject-matter experts on supplier risk acceptance, remediation, continuity, transition, and exit decisions.
• Monitor supplier performance, track KPIs, and elevate quality issues when appropriate.
• Coordinate and/or execute supplier audits, manage findings, initiate quality records, and ensure timely CAPA closure.
• Maintain supplier data in quality systems (e.g., Veeva, TrackWise) to ensure accuracy and inspection readiness.
• Engage with suppliers to align requirements, governance and process improvement initiatives.
• Ensure compliance with procedures, perform quality checks, and contribute to continuous improvement.
• Collaborate with internal teams (R&D, Supply Chain, Sourcing, QA) to assist in the development and execution of supplier quality strategies.

Travel

Up to 10% domestic and international travel may be required for supplier engagements and audits.

What we expect of you

Basic Qualifications:

• Doctorate degree OR
• Master’s degree and 2 years of Science, Engineering, or experience in a related field OR
• Bachelor’s degree and 4 years of Science, Engineering, or experience in a related field OR
• Associate’s degree and 8 years of Science, Engineering, or experience in a related field OR
• High school diploma / GED and 10 years of Science, Engineering, or experience in a related field

Preferred Qualifications:

• Master’s degree or equivalent in Life Sciences or Engineering.
• Knowledge of GxP, ISO standards, and regulatory expectations for R&D suppliers.
• Experience with supplier quality risk assessment tools and audit practices.
• Working knowledge of computerized system validation and assurance principles, risk-based system lifecycle practices, and applicable expectations for electronic records, electronic signatures, audit trails, and data integrity.
• Experience assessing or overseeing GxP technology suppliers, including software, software-as-a-service, cloud, hosting, infrastructure, implementation, validation, and managed service providers.
• Ability to evaluate supplier audit reports, validation plans and reports, requirements and traceability, testing evidence, security and continuity controls, change records, deviations, CAPAs, and service performance data.
• Experience and proficiency in overseeing AI-enabled GxP systems, including risk assessment, governance, validation, data integrity, and ongoing supplier monitoring.
• Excellent written and verbal communication skills.
• Ability to work effectively in cross-functional teams and in a matrixed environment.
• Strong problem-solving and critical thinking abilities.
• Detail-oriented with a continuous improvement mindset.
• Proactive collaboration and relationship-building skills.
• Ability to manage multiple priorities and deliver results under timelines.

What you can expect from us

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Salary Range 104,287.35USD -141,094.65 USD