GCP Quality Compliance Manager

Amgen; Uxbridge; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading biotechnology company in the UK is seeking a GCP Quality Compliance Manager. This role involves maintaining the Quality Management System (QMS), ensuring compliance with GCP standards, and analyzing quality metrics. Candidates should have a degree and experience in Quality Management within the pharmaceutical or biotechnology sectors. The position allows flexibility with remote work options from Uxbridge or Cambridge.

Benefits

Generous Total Rewards Plan

Opportunities for professional growth

Inclusive community

Work/life balance benefits

Qualifications

• Previous experience in Quality Management or Quality Assurance in the pharmaceutical/biotech industry.
• Thorough understanding of Clinical R&D activities, Global Regulations, and GCP.
• Experience with risk-based quality management.

Responsibilities

• Maintain and improve the Quality Management System (QMS).
• Collect, analyze, and report quality metrics.
• Ensure compliance with GCP standards.

Skills

Quality Management

Analytical skills

Communication skills

Critical thinking

Collaborative abilities

Education

Degree education

Job description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

GCP QUALITY COMPLIANCE MANAGER

LIVE

What you will do

In this vital role you will provide critical support to the Process Quality function by assisting in the implementation, monitoring, and continuous improvement of Amgen’s R&D Quality Management System (QMS) and Regional Quality Oversight.

• Maintain and improve the QMS by tracking, documenting, and implementing quality initiatives to meet regulatory requirements.
• Collect, analyze, and report quality metrics (KPIs/KQIs) to identify trends, risks, and opportunities for improvement.
• Ensure compliance with GCP standards and regulatory requirements across R&D.
• Act as liaison between Process Quality and Global Networks to enable smooth collaboration.
• Provide quality oversight at key sites, including readiness checks (remote/onsite) and risk assessments for audits.
• Identify data quality gaps, recommend and implement corrective actions.
• Coordinate and support inspections and audits (preparation, conduct, closeout, and responses).
• Apply project management, root cause analysis, and corrective/preventive action follow-up.
• Integrate data, trends, and insights into plans and recommendations.
• Act as a subject matter expert in GCP and SOP/Standards management.

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:

• Degree educated
• Previous experience in Quality Management, Quality Assurance, or other relevant areas of the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility
• Thorough understanding of Clinical R&D activities, Global Regulations and GCP
• Strong analytical, critical thinking, collaborative and decision-making abilities
• Excellent written and verbal communication skills

THRIVE

What you can expect of us

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

• Vast opportunities to learn and move up and across our global organization
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

LOCATION: Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace. Onsite domestic travels required.

APPLY NOW

for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

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.