Quality Compliance Manager

HOW MIGHT YOU DEFY IMAGINATION?At Amgen, every challenge is an opportunity. 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 read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.Quality COMPLIANCE manager LIVEWHAT YOU WILL DOWe are hiring a Quality Compliance Manager, which will operate within the General Medicine Therapeutic Area.In this vital role you will provide proactive end to end quality support for the development andimplementation of a risk-based quality assurance strategy that advances quality by design principles for the full clinical development program. (protocol development, database lock, and regulatory submissions / approvals).Reporting to the Quality Compliance Director, you will oversee quality management and ensure compliance for global and local clinical trials by supporting study teams and trial sites involved in Amgen-sponsored Trials.RESPONSIBILITIESGCP Subject Matter Expert - Provide independent and objective quality advice in support of clinical trial activities and in line with current best practice.Provide quality oversight for Amgen programmes for all stages of products in clinical developmentEnsure quality oversight for the Risk Assessment Categorization Tool (RACT) for each trial to guarantee the proper identification, prioritization, and mitigation of risks to critical data and processes and patient safety, welfare and rightsSupport the establishment of regional expertise to ensure quality and compliance to local RegulationsSupport Clinical Trial Teams for all quality management activities, including Deviations / CAPAs, Inspection Readiness and Management activities, and Serious Breaches / Privacy IssuesEnsure TA-specific data integrity, including technologies for data collection and measurement (e.G., biomarker usage and imaging methods)Review clinical trial protocols ensuring simplification, application of lessons learned, and identification of critical data and processesDemonstrated ability to leverage artificial intelligence (AI) tools and technologies to streamline workflows, drive process automation, and support data-driven decision-making. Must be adept at identifying opportunities to apply AI for operational efficiency and continuous improvement initiatives.Manage / support regulatory inspection and review responses.Prepare, analyze and Identify data quality indicators / trends, identify areas of weakness / gaps, recommend and implement corrective actions and communicate quality metrics and other significant quality information on periodic basis to key stakeholdersSupport Monthly meetings with program level CPO senior management / associate directors to review, but not limited to, the following : on-going quality issues, quality trends, program filing timelines and potential inspections.Support response generation for audit findings and self reported deviations.Support the establishment of regional expertise to ensure quality and compliance to local regulationsProvide Study Specific Vendor Quality Oversight Prepare, analyze and Identify data quality indicators / trends, identify areas of weakness / gaps, recommend and implement corrective actions and communicate quality metrics and other significant quality information on periodic basis to key stakeholdersPlan, conduct and report out on risk-based Good Clinical Practices (GCP) audits (investigator site audits, affiliate audits, and study level audits)WINWHAT WE EXPECT OF YOUWe are all different, yet we all use our unique contributions to serve patients. The individual we seek has technological literacy and leadership skills, and has these qualifications : 8-13 years of Experience in Quality Management, Quality Assurance or other relevant areas of thepharmaceutical / biotech industry where risk-based quality and quality by design are a coreresponsibilityOversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Track wise. Thorough understanding of Clinical R&D activities and Global Regulations.Knowledge of the Regulatory Submission and Inspection Management procedures.Quality Oversight of Clinical Trials, including clinical trial protocol development, execution, and submissions. Excellent verbal and written communication skills, including strong business writing abilities and active listening.Ability to transform business and stakeholder feedback into clear, efficient processes using a straightforward language and format.Strong analytical, critical-thinking, and decision-making abilities.Capability to understand and articulate technical concepts and literature in spoken and written English.THRIVEWHAT YOU CAN EXPECT OF USVast 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 NOWFOR A CAREER THAT DEFIES IMAGINATIONIn our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.CAREERS.AMGEN.COMEQUAL OPPORTUNITY STATEMENTAmgen 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 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 accommodation.