Pharma Data Engineer - Databricks AWS
Indexed description
Key Responsibilities
Design, build, and maintain scalable ETL/ELT pipelines (batch and streaming) using Databricks, AWS, and related orchestration tools
Write and optimize advanced SQL, and build data transformations in Python or Scala
Integrate external data sources via APIs and manage pipeline orchestration (Airflow, Databricks Workflows, AWS Glue)
Apply data quality, governance, cataloging, and lineage practices aligned with regulated-industry standards
Work within GxP-regulated data environments and apply awareness of data privacy/compliance considerations (e.g., 21 CFR Part 11, GDPR where applicable)
Partner with business stakeholders across the pharma value chain (R&D, Manufacturing & Quality, Commercial, Drug Development) to gather and translate requirements into technical specifications
Present technical work and data strategy to executive-level audiences
Prioritize high-impact data initiatives and proactively identify and avoid duplicated data efforts
Support change management and adoption of new data solutions across business teams. Help stand up new data domains from scratch (green-field build), not just maintain existing ones
Requirements
Required Qualifications
Data Engineering & Pipelines
- Data Engineering & Pipelines
- ETL/ELT development (batch and streaming)
- Advanced SQL (joins, window functions, query optimization)
- Python or Scala for data transformation
- Data pipeline orchestration (Airflow, Databricks Workflows, AWS Glue)
- API integration for external data source ingestion
- Databricks (Delta Lake, Unity Catalog, Genie)
- Cloud platforms — AWS (S3, Glue, Athena) and/or Azure/Google Cloud Platform equivalents
- Data warehousing concepts (dimensional modeling, star schema)
- BI/visualization tools (Tableau, Power BI, or similar) to understand downstream consumption
- Data profiling and cleansing techniques
- Metadata management and data cataloging
- Master data management (MDM) principles
- Data lineage tracking
- Data governance frameworks (especially regulated-industry standards)
- Familiarity with GxP-regulated data environments
- Understanding of the pharma value chain (R&D, Manufacturing & Quality, Commercial, Drug Development)
- Awareness of data privacy/compliance considerations (21 CFR Part 11, GDPR where applicable)
- Knowledge of common pharma data domains (clinical, manufacturing, quality, commercial)
- Requirements gathering and translation (business need → technical spec)
- Cross-functional communication (Business ↔ IT)
- Executive-level presentation skills (given EC visibility)
- Change management / adoption support
- Prioritization frameworks (identifying high-impact vs. low-value data asks)
- Cost-avoidance mindset (spotting duplication before it happens)
- Ability to work with ambiguity and evolving priorities
- Agile/Scrum familiarity
- Documentation discipline (data dictionaries, source-to-target mappings)
- Vendor/partner coordination (if external data sources are involved)
- Prior consulting or client-facing delivery experience
- Experience standing up new data domains from scratch (green-field vs. maintenance)
- Familiarity with AI/GenAI-enabled analytics tools
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