R&D Supplier Quality Manager Lisboa

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We’re proud to be ranked the #1 company in Best Workplaces (category 201–500 employees) by the Great Place to Work Institute in Portugal. At our Lisbon office, located in the heart of the city, we foster innovation, excellence, and inspiration. With over 300 talented professionals from more than 35 nationalities, we’re shaping the future of healthcare across diverse areas such as Cybersecurity, Data & Analytics, Digital Innovation, Finance, HR, Regulatory Affairs, and more. Come thrive with us at Amgen, supporting our mission: To Serve Patients. What we do here truly matters in people’s lives.

R&D Supplier Quality Manager

LIVE

What you will do

Amgen’s R&D Quality team is building a robust Supplier Quality Oversight capability to proactively identify and prevent critical quality issues across our supplier network.

As R&D Supplier Quality Manager, you’ll report to the Director or Sr. Manager of Supplier Quality Management within Precision Medicine, Diagnostics and Supplier Quality (PMDSQ). You’ll be responsible for the operational execution of supplier quality processes for R&D suppliers under GCP, GLP, and GPv
P regulatory frameworks.

This
- on role involves quality oversight of global and local
- party suppliers, ensuring compliance, mitigating risks, and driving continuous improvement throughout the supplier lifecycle — from onboarding to audits, issue management, and offboarding.

You’ll support all categories: GMP clinical, GLP
- clinical, and pharmacovigilance, working
- functionally with Supply Chain, Procurement, QA, and external partners.

Key Areas of Responsibility:

• Conducting
  - based supplier assessments, managing quality agreements, and ensuring regulatory compliance
• Supervising supplier performance via KPIs and quality metrics, identifying trends and escalating issues
• Coordinating and executing supplier audits, managing findings, CAPAs, and inspection readiness
• Maintaining supplier data in electronic quality systems (e. g. , Veeva, Track
  Wise)
• Supporting training implementation, documentation standards, and continuous improvement initiatives
• Building collaborative relationships with internal teams and external suppliers
• Willingness to travel up to 15%

What we expect of you

We value diverse perspectives and outstanding contributions. The ideal candidate is disciplined, organized, and analytical, with strong
- solving skills and a proactive mindset.

Basic Qualifications

• Doctorate degree OR
• Master’s degree and 3 years of relevant experience OR
• Bachelor’s degree and 5 years of relevant experience OR
• Associate’s degree and 10 years of relevant experience OR
• High school diploma / GED and 12 years of relevant experience

You must also have experience managing people and/or leading teams, projects, or programs.

Preferred Qualifications

• Experience in pharma/biotech or medical device industry in a quality management role
• Exposure to clinical research environments with quality oversight responsibilities
• Experience in supplier quality management, audits, and CAPA processes
• Familiarity with Gx
  P and ISO standards applicable to R&D suppliers
• Strong project management and
  - functional collaboration skills
• Working knowledge of GCP, GLP, GPv
  P regulations and trends
• Experience implementing new regulations, conducting gap assessments, and improving QMS processes

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and
- being.

• Vast opportunities to learn, develop, and move up and across our global organization.
• A diverse and inclusive community of belongings, where colleagues are empowered to bring ideas to the table, try new things, and act.
• Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth, and career benefits.
• Flexible work arrangements.

Apply Now

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Equal opportunity statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.

Seniority level

• Not Applicable

Employment type

• Full-time

Job function

• Quality Assurance
• Industries: Biotechnology Research and Pharmaceutical Manufacturing

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