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Senior Associate, Quality Compliance

India, Hyderabad · Job Posted February 20, 2026
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Job Description

The senior associate will work within R&D Quality’s Business Intelligence and Data Analytics (BIDA) team to help deliver actionable information and recommendations to key leaders and stakeholders by maintaining and expanding our data pipelines, tools, and reporting. This role contributes to ensuring Amgen’s pursuit of life-saving medication is done with the highest regard for quality and compliance to regulations.

Job Responsibility

  • Extract and clean data from internal systems for regular and ad hoc reporting, including data pipeline creation and maintenance
  • Generate, validate, and deliver KPIs, quality metrics, and performance indicators used across the R&D Quality landscape
  • Investigate and analyze metric trends, anomalies, and operational insights
  • Design, build, and maintain Tableau dashboards for operational monitoring, compliance reporting, and executive summaries
  • Develop and maintain Python scripts used for data processing, transformation, and report automation
  • Help create reusable components for common data analysis tasks and documentation
  • Ensure version control and proper documentation of scripts and workflows

Requirements

  • Master’s degree and 7-10 years in Pharma and Biotechnology R&D Quality
  • Bachelor’s degree and 10-15 years of years in Pharma and Biotechnology R&D Quality
  • Exceptional attention to detail and accuracy in all deliverables
  • Ability to work independently and proactively in a fast-paced environment
  • Proficiency with Tableau or similar data visualization tools
  • Proficiency with Python or other object-oriented programming language
  • Proficiency with SQL and Databricks
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams)
  • Effective communication, critical thinking and problem-solving
  • Experience in conducting data analyses and translating data sets into actionable insights

Nice to have

  • Familiarity with project management tools and methodologies
  • Knowledge of GCP, GLP, GPvP, and/or the conduct of clinical trials
  • Familiarity with Databricks and SQL
  • Experience working in a multinational environment with global teams
  • Experience within Biotech/pharmaceutical Research
  • Independent and teamwork capabilities

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