Senior Associate, Quality Compliance (Analytics)

Biopharma Careers; Hyderabad; On-site; INR 1,200,000 - 2,100,000; Full time

Job summary

Amgen seeks a Senior Associate Quality Compliance (Analytics) to join the R&D Quality BI/Data Analytics team in Hyderabad. You will maintain and expand data pipelines, build dashboards, and deliver actionable insights to leaders and stakeholders, ensuring quality and regulatory compliance.

Ideal candidates have a Master’s in Pharma or Biotechnology with 3–5 years in R&D Quality, or a Bachelor’s with 6–9 years in Pharma/BI R&D Quality, plus expertise in Tableau, Python, and SQL.

Qualifications

• Master’s degree and 3–5 years in Pharma or Biotechnology R&D Quality, or Bachelor’s degree with 6–9 years in Pharma/BI R&D Quality.
• Experience with data pipelines, dashboards and reporting.
• Proficiency with Tableau or similar data visualization tools and Python scripting.

Responsibilities

• Extract and clean data from internal systems for regular and ad hoc reporting.
• Generate, validate, and deliver KPIs and quality metrics across R&D Quality.
• Design, build, and maintain Tableau dashboards for monitoring and executive summaries.

Skills

Tableau

Python

SQL

Databricks

Data visualization

Microsoft Office

Education

Master’s degree in Pharma/Biotech

Bachelor’s degree in Pharma/Biotech

Tools

Tableau

Python

SQL

Databricks

Job description

Career Category

Quality

Job Description

Role Name: Senior Associate Quality Compliance (Analytics)

Department Name: R&D Quality

Role GCF: 4

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

ABOUT THE ROLE

Role 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.

Roles & Responsibilities

• 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.
• Follow GxP controls and proper documentation of scripts and workflows.

Basic Qualifications and Experience

• Master’s degree and 3-5 years in Pharma (or) Biotechnology R&D Quality OR
• Bachelor’s degree and 6-9 years of years in Pharma (or) Biotechnology R&D Quality.

Functional Skills

• Must-Have Skills:
  • 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
• Good-to-Have Skills:
  • Familiarity with project management tools and methodologies
  • Knowledge of GCP, GLP, GPvP, and/or the conduct of clinical trials
  • Experience working in a multinational environment with global teams
  • Experience within Biotech/pharmaceutical Research
  • Independent and teamwork capabilities

Soft Skills

• Excellent verbal and written communication skills
• High degree of professionalism and interpersonal skills
• Strong problem-solving abilities and adaptability to changing priorities
• Collaborative mindset and ability to build positive relationships across diverse teams
• Resilience, discretion, and the ability to thrive under pressure

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 with 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.