Quality Compliance Senior Manager

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. QUALITY COMPLIANCE SENIOR MANAGER LIVE What you will do In this vital role you will provide proactive end to end quality support for the development and implementation of a risk-based quality assurance strategy, for all stages of products in the clinical development program. You will support global and local study teams and all clinical trial sites who participate in Amgen sponsored trials. Serve as a Good Clinical Practices (GCP) Subject Matter Expert, providing independent quality guidance for clinical trials Plan, conduct and report out on risk-based GCP audits (investigator site audits, affiliate audits, service provider audits, and study level audits) or support outsourced audits Manage quality events and regulatory inspections, and advise on responses, including root cause analysis and CAPA plans Ensure quality oversight for the Risk Assessment Categorization Tool (RACT) to identify and mitigate trial risk Support monthly meetings with clinical program leaders to review quality and compliance risks, including deviations, trends, filing timelines, inspections, and cross-program risks Conduct new vendor qualifications in a risk-based manner Analyze data quality trends, address areas of weakness and gaps, implement and communicate key quality metrics Coordinate and support key technologies for data collection and measurement (e.g., biomarker usage and imaging methods) Be part of our team You will be joining a dynamic and growing team that operates within General Medicine Therapy Area, reporting to the Therapeutic Area Quality Lead. 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: Experience in Quality Management, Quality Assurance, or other relevant risk-based quality practices in the pharmaceutical/biotech industry Expertise in Quality Management Systems (QMS), including electronic systems like Veeva or TrackWise Strong knowledge of Clinical R&D, global regulations and regulatory submissions Quality Oversight of Clinical Trials, including protocol development, execution and submissions Experience within GCP, including conducting audits and managing inspections Excellent communication, active listening, strong analytical and decision-making skills Leadership or mentoring experience is considered a plus Degree educated 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. 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.

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