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GCP Quality Auditor

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GCP Quality Auditor

Portugal - Lisbon Apply Now
JOB ID: R-225691 ADDITIONAL LOCATIONS: Portugal - Lisbon WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Oct. 07, 2025 CATEGORY: Quality

Join our team at AMGEN Capability Center Portugal, number 1 company in Best WorkplacesTM https://www.greatplacetowork.pt/ ranking in Portugal in 2024 (category 201-500 employees) by the Great Place to Work Institute. We have a team of over 500 talented people and more than 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data & Analytics, Digital, Technology and Innovation, Finance, General & Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives.

GCP QUALITY AUDITOR

LIVE

WHAT YOU WILL DO

You will be joining Amgen’s R&D Quality Audit Team of expert, professional and widely experienced individuals working with a global remit across Amgen’s portfolio in all stages of development and post marketing. The R&D Quality audit team is part of Amgen's R&D Quality Group. 

In this vital role as GCP Quality Auditor within R&D Quality you will be planning and participating in global audits of Amgen’s clinical trials activities. You may also support regulatory inspections of clinical sites and Amgen facilities.

The responsibilities of the role will include:

  • Plan, conduct and report routine and directed GCP compliance audits internationally
  • Serve as a lead auditor for complex GCP audits
  • Identify and communicate compliance risks to R&D Quality management
  • Host and/or play a role in regulatory authority inspections
  • Contribute to or lead R&D Quality process improvement initiatives
  • Author and contribute to the development of R&D Quality cross functional controlled documents

The role can entail up to 40% travel to international destinations.

WIN

WHAT WE EXPECT OF YOU

We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional are these qualifications and skills:

Minimum requirements

  • ​Bachelor’s degree in a scientific discipline, medical sciences or pharmacy qualification
  • Proven and extensive international auditing experience in GCP
  • Experience of data mining, manipulation and data analytics would be advantageous
  • Excellent written and verbal English communication skills

Preferred requirements

  • Postgraduate qualification
  • Experience supporting regulatory authority inspections
  • Participation in process improvement initiatives

THRIVE

WHAT YOU CAN EXPECT OF US

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

APPLY NOW
Objects in your future are closer than they appear. Join us.

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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, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Apply Now
Live. Win. Thrive.

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