Associate Scientific Technical Engineer II, PDS&T CMC
$66K/yr – $126K/yr
You'll complete your application on the employer's website.
$66K/yr – $126K/yr
You'll complete your application on the employer's website.
Job type
Salary
$66K/yr – $126K/yr
Location
Sector
Posted
19 days ago
AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues across areas including immunology, oncology, and neuroscience. The Associate Scientific Technical Engineer II will design, build, and operate production-grade data pipelines and data products supporting AI/ML, analytics, and automation across CMC and manufacturing. The role integrates and harmonizes data from manufacturing and development systems while enabling governed, reliable data assets for scientists, engineers, and AI systems.
Responsibilities
Design and implement scalable, robust data ingestion pipelines that connect CMC and manufacturing source systems — including MES (Manufacturing Execution Systems), process historians, LIMS, QMS, ERP platforms, and instrument data sources — to centralized and federated data environments
Build connectors, adapters, and integration layers that handle the heterogeneous data formats, protocols, and latency profiles characteristic of pharmaceutical manufacturing environments
Support both batch and real-time/streaming data patterns, selecting appropriate architectures based on use case requirements
Develop and maintain harmonized data models and ontologies that bring consistency to CMC and manufacturing data across sites, systems, and modalities
Execute semantic mapping efforts that align source system fields, units, and identifiers to enterprise data standards and scientific meaning
Collaborate with process scientists, analytical chemists, and manufacturing engineers to ensure data models accurately reflect domain reality
Implement automated data quality controls, validation frameworks, and anomaly detection mechanisms across pipeline layers
Build and maintain data lineage documentation and metadata infrastructure, enabling full traceability from source system to AI model input
Establish pipeline observability practices — monitoring, alerting, SLA tracking — to ensure data product reliability in production
Support data governance practices aligned with GxP requirements, 21 CFR Part 11, and AbbVie data standards
Architect and deliver governed, versioned, reusable data products purpose-built for AI/ML consumption, including feature stores, curated datasets, and vector-ready data layers for RAG and LLM applications
Partner closely with data scientists, ML engineers, and process modelers to understand model data requirements and translate them into reliable, scalable data infrastructure
Accelerate AI program delivery by eliminating data bottlenecks — not by workarounds, but by solving root causes structurally
Contribute to the design and evolution of PDST's cloud-based data platform, including lakehouse architecture, data cataloging, access control, and compute infrastructure
Write and maintain infrastructure-as-code, CI/CD pipelines, and automated testing frameworks for data systems
Support platform onboarding of new CMC data domains and manufacturing sites, ensuring consistent application of standards and patterns
Provide operational support for production data pipelines, maintaining uptime and data freshness commitments
Influence technical decision-making without formal authority — earning trust through scientific rigor, transparent methodology, and demonstrated business impact
Preferred
Experience in pharmaceutical, biotech, or other regulated life sciences manufacturing environments
Familiarity with GxP data principles, 21 CFR Part 11 compliance, or data integrity requirements in regulated industries
Prior exposure to manufacturing source systems such as MES, process historians (e.g., OSIsoft PI/AVEVA), LIMS, QMS, or ERP platforms
Experience building data infrastructure for AI/ML programs — including feature engineering pipelines, model training datasets, or vector/embedding data layers for RAG architectures
Regulated life sciences manufacturing
GxP data principles
21 CFR Part 11 compliance
Regulated data integrity
MES
OSIsoft PI/AVEVA
LIMS
QMS
ERP platforms
AI/ML data infrastructure
Feature engineering pipelines
Model training datasets
Vector
embedding data layers
RAG architectures
Benefits
Paid time off (vacation, holidays, sick)
Medical, dental, and vision insurance for eligible employees
401(k) for eligible employees
Eligibility to participate in short-term incentive programs
Company
Global biopharmaceutical company developing medicines for immunology, oncology, neuroscience, aesthetics.
North Chicago, Illinois, USA
https://www.abbvie.com/
Founded in 2013
10001+ employees
Qualifications
Bachelor's Degree in Computer Science, Data Engineering, Information Systems, Software Engineering, Bioinformatics, or a closely related technical field plus 2 years' experience OR Master's Degree with 0 years' experience
Respective years of hands-on experience designing and building enterprise-grade data pipelines, integration workflows, and data products in complex, multi-source environments
Expert-level proficiency in Python for data engineering tasks — pipeline development, transformation logic, data validation, and automation
Strong SQL skills across modern analytical and transactional databases; comfort with both ANSI SQL and platform-specific dialects
Demonstrated experience with cloud data platforms (AWS, Azure, or GCP) and modern data stack components — including tools such as dbt, Spark, Airflow, Databricks, Snowflake, or equivalents
Develop ETL/ELT pipelines using tools such as Informatica, Talend, Apache NiFi, and cloud-native services (e.g., AWS Glue, Azure Data Factory)
Implement master data management (MDM), metadata management, and data cataloging solutions to ensure proper data lineage, accessibility, and compliance
Set and enforce standards for API development and data integration (REST, GraphQL, OData), enabling seamless integration using microservices architectures
Design logical, physical, and conceptual data models using modeling tools (e.g., Erwin, PowerDesigner, dbt)
Ownership orientation: you define your own problem space, drive solutions to completion, and hold yourself accountable to outcomes — not just outputs
Solution-architect instinct: you think before you build, consider the full landscape of available approaches, and choose tools based on fit-for-purpose reasoning rather than familiarity or trend
Scientific integrity: you build models you can explain, defend, and improve — and you apply the same standard to the work of others
Influence through credibility: you earn the confidence of scientists, engineers, and quality professionals by being right, being clear, and being useful — not by title or volume
Bias for impact: you are drawn to problems where the stakes are high and the analytical opportunity is real, and you are energized rather than intimidated by ambiguity
Experience in pharmaceutical, biotech, or other regulated life sciences manufacturing environments
Familiarity with GxP data principles, 21 CFR Part 11 compliance, or data integrity requirements in regulated industries
Prior exposure to manufacturing source systems such as MES, process historians (e.g., OSIsoft PI/AVEVA), LIMS, QMS, or ERP platforms
Experience building data infrastructure for AI/ML programs — including feature engineering pipelines, model training datasets, or vector/embedding data layers for RAG architectures
Bachelor's Degree in Computer Science, Data Engineering, Information Systems, Software Engineering, Bioinformatics, or a closely related technical field plus 2 years’ experience OR Master’s Degree with 0 years' experience.
Required skills
Data Pipeline Engineering, Python, SQL, Cloud Data Platforms, ETL/ELT, Databricks, Apache Spark, Apache Airflow, Snowflake, Master Data Management, Data Modeling, API Integration REST, API Integration GraphQL, API Integration OData
Experience
2+ years
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