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Amgen

Makes biotech medicines for serious illnesses

Quality Compliance Senior Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRemote in USARemote

About the Job

Requirements

  • A doctorate degree and 2 years of Quality experience, or a master's degree and 4 years of Quality experience, or a bachelor's degree and 6 years of Quality experience, or an associate's degree and 10 years of Quality experience, or a high school diploma or GED and 12 years of Quality experience.
  • A bachelor's degree in a scientific, clinical, quality, data, or related discipline, with substantial relevant experience in R&D Quality, clinical development, clinical operations, quality systems, risk management, or centralized monitoring.
  • Demonstrated experience leading and developing professional employees or leading complex cross-functional teams.
  • Experience interpreting quality, operational, or risk data and converting findings into clear recommendations, escalations, and follow-up actions.
  • Working knowledge of GCP, quality-risk management, issue management, CAPA and deviation processes, audit and inspection readiness, and quality governance.
  • Experience as an R&D Quality process owner or in quality oversight across deviations, CAPAs, audits, inspections, management review, or risk-management processes.
  • Experience with QMS platforms, dashboards, data visualization, data quality, business analysis, user acceptance testing, or digital-product implementation.
  • Experience with risk-based quality management, centralized monitoring, KRIs, QTLs, CSM, or signal-based quality oversight.
  • Experience working with AI-enabled analytics or digital quality products, including critically evaluating system-generated insights and applying appropriate human judgment.
  • Experience leading operational change in a global matrix environment.

Responsibilities

  • Lead the day-to-day operation of the QuIC function and manage a professional team responsible for portfolio-level quality monitoring.
  • Own and continuously improve the QuIC operating model, including review cadence, signal triage, documentation expectations, escalation pathways, action tracking, and governance routines.
  • Establish consistent review cadences and business standards for evaluating dashboard outputs, quality metrics, trends, anomalies, threshold breaches, and other QuIC-generated signals.
  • Lead the review and prioritization of dashboard outputs, quality metrics, trends, anomalies, and threshold breaches to identify issues requiring further assessment or follow-up.
  • Translate complex quality information, including deviations, CAPAs, audit and inspection insights, operational metrics, and related evidence, into clear, governance-ready summaries, recommendations, and escalations.
  • Ensure that significant findings are appropriately documented, escalated, and routed to accountable process owners and cross-functional stakeholders.
  • Define and propose QuIC business rules, operating standards, documentation expectations, escalation pathways, and workflow requirements; ensure changes requiring controlled approval are reviewed through the appropriate accountable Quality governance.
  • Partner with R&D Quality, Global Development Operations, and other stakeholders to ensure QuIC insights are understood and acted upon.
  • Lead process improvements and provide business leadership for QuIC enhancements, including signal definitions, thresholds, business rules, data-quality expectations, training, and adoption activities.
  • Monitor the effectiveness, timeliness, quality, and capacity of oversight activities and implement practical improvements where needed.
  • Ensure activities comply with applicable GxP, quality-system, data-governance, and internal procedural requirements.

Desired Qualifications

  • Strong communication, stakeholder-management, organizational, and decision-making skills.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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