Scientific Technical Engineer - PDS&T CMC
BioSpace
About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube. Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube. Job Description While the AI innovation race in Biopharma is focused on Drug discovery, Product Development/ CMC represents the next barrier/ bottleneck. The complexity of biological systems, the rigor of regulatory expectations, the pace of pipeline growth, and the enormous value at stake make this one of the highest-leverage domains for applied data science and AI in the entire pharmaceutical value chain. We here at BTS - PDST, are building a dedicated, AI-native team that is driving cutting edge programs across early stage, late stage and commercial product development to accelerate E2E product development and launch, maximize yields of block buster products. Through our deep collaboration with PDST scientists we are boldly reimagining how Abbvie can bring our pipeline products and lifesaving drugs to patients faster, safer and in cost effective manner fueled by AI. Principal Data Engineer is a highly technical, AI-native role responsible for designing, building, and operating production-grade data pipelines and data products that power AI/ML, analytics, and automation across AbbVie's CMC and manufacturing ecosystem. This role is embedded inside PDST and works at the frontier of pharmaceutical data engineering. You will integrate and harmonize data from the full spectrum of manufacturing and development systems including MES, historians, LIMS, QMS, ERP, and instrument platforms and transform it into reliable, governed, semantically rich data assets that data scientists, process engineers, and AI systems can actually use. Responsibilities Data Ingestion & Integration Enterprise-scale scope: Enterprise-scale biologics portfolio spanning clinical, commercial, and lifecycle stages Building AI playbook for the future: First-in-AbbVie and first-in-biologics analytical approaches; you build the AI playbook for the future Growth and Impact: Direct impact on regulatory submissions, commercial readiness, and manufacturing decisions through deep cross-functional exposure to manufacturing, quality, regulatory, and scientific leadership Mission: Every model you build helps ensure safe, reliable medicines reach patients at scale Data Harmonization & Semantic Modeling 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. Data Quality, Observability & Governance 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. AI/ML Enablement & Data Product Development 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. Platform & Operational Enablement 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. Stakeholder Engagement & Scientific Leadership Influence technical decision-making without formal authority earning trust through scientific rigor, transparent methodology, and demonstrated business impact. Qualifications Required Bachelors Degree Computer Science, Data Engineering, Information Systems, Software Engineering, Bioinformatics, or a closely related technical field plus6 years experience; Masters Degree plus5 years experience; PhD plus0 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. 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. Preferred 3+ years of hands-on experience designing and building enterprise-grade data pipelines, integration workflows, and data products in complex, multi-source environments. Familiarity with technology transfer workflows, process characterization study design, or commercial process validation (PPQ/PV) in a biologics or pharmaceutical context. 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. Knowledge of biologics manufacturing processes (e.g., upstream cell culture, downstream purification, fill-finish) or CMC development workflows. Familiarity with data mesh, data fabric, or federated data architecture patterns. Experience with graph databases, knowledge graphs, or ontology frameworks applied to scientific or manufacturing data. Contributions to open-source data tooling or demonstrated engagement with the modern data engineering community. Design logical, physical, and conceptual data models using modeling tools (e.g., Erwin, PowerDesigner, dbt). Additional Information The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees. This job is eligible toparticipatein our short-term incentiveprograms. Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or anyother formofcompensation andbenefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Companys sole and absolute discretion, consistent withapplicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: #J-18808-Ljbffr BioSpace
- ...Drug discovery, Product Development/ CMC represents the next barrier/ bottleneck... ...manner fueled by AI. Principal Data Engineer is a highly technical, AI-native role responsible for... ...manufacturing, quality, regulatory, and scientific leadership Mission: Every model you...ScientificTemporary work
- ...within the Targeted LNP (tLNP) CMC Team at AbbVie is dedicated... ...cross-functional leader for scientific leadership in the development... ..., Process Chemistry, Process Engineering, Drug Product Development, and... ...scientist, generating original technical ideas and research or...ScientificFull timeLocal area
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- ...discovery, Product Development/ CMC represents the next barrier/... ...role built for a scientist-engineer who thinks in systems, builds... ...with purpose, and leads through technical credibility. This role is a... ..., quality, regulatory, and scientific leadership Mission: Every...ScientificFull timeLocal area
- ...Development Science and Technology (PDS&T) Analytical group is... ...and product development, CMC, process engineering, internal and external... ...critical experiments to answer scientific questions. Understand the... ...development and validations, technical transfer packages, and...ScientificFull timeTemporary workLocal area
- ...discovery, Product Development/ CMC represents the next barrier/... ...role built for a scientist-engineer who thinks in systems, builds... ...with purpose, and leads through technical credibility. This role is a... ..., quality, regulatory, and scientific leadership Mission: Every...ScientificFull timeLocal area
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- ...experimental approaches to solve difficult scientific and technical challenges. Working with discovery,... .... Collaborate to ensure successful CMC interactions with regulatory... ...organic chemists, analytical chemists, engineers, drug metabolism scientists, formulators...ScientificWork experience placement
- ...mentor, guide, and supervise scientific personnel while fostering collaborations... ..., Process Chemistry, Process Engineering, Drug Product Development,... ..., Quality Assurance and CMC-Regulatory. Key... ...documents, laboratory data, technical memos and reports. The position...Scientific
- ...develop & advocate strategic positions for CMC regulatory/CMC issues with cross... ...and external groups and serving as a scientific/technical resource within RA CMC that provides guidance... ...in pharmacy, biology, chemistry, Engineering or related subjects. Preferred Education...ScientificFull timeLocal area
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$109.5k - $208.5k
...Job Title Conceive and execute novel scientific research or development in Clinical Pharmacology... ...of investigator brochures, common technical documents, white papers, and other... ...clinical pharmacology position to clinical, CMC and regulatory teams. Author scientific...ScientificWork at officeLocal areaImmediate startRemote workMonday to Friday$109.5k - $208.5k
...the Product Development and CMC teams and will collaborate with... .... Initiate and/or support scientific initiatives to drive innovation... ..., Chemistry, Chemical Engineering, or related disciplines with:... ...influence without authority, drives technical excellence, and inspires...ScientificFull timeTemporary work- ...science organization responsible for all CMC analytical activities related to the... ...Solves difficult and highly complex technical issues in an evolving regulatory landscape... ...manufacturing and controls Manages and develops scientific talent (20-30 Scientist, Senior...ScientificFull time
- ...Develop/align local processes/workflows and GMP approaches within PDS&T LC and global processes in close cooperation with other PDS&T... ...thorough theoretical and practical understanding of own scientific discipline. Minimum 3 years of experience in the pharmaceutical...ScientificFull timeContract workTemporary workLocal areaShift work
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- ...ideal candidate will bring broad technical expertise and a strong... ...including Process Chemistry, Process Engineering, Drug Product Development,... ..., Quality Assurance, and CMC-Regulatory. Responsibilities... .... Understand relevant scientific literature and apply theoretical...ScientificFull timeTemporary workLocal area
$35 - $37.48 per hour
...Laboratory Testing Specialist Uses scientific education and analytical chemistry experience to perform simple to moderately complex laboratory testing within a good manufacturing practices laboratory to generate results. Interprets data output to determine conformance...ScientificHourly payContract work- ...motivated person who can make scientific contributions across... ...functional project teams establishing CMC program strategy for clinical... ...documents, laboratory data, technical reports and internal/external... ...chemists, analytical chemists, engineers, drug product development,...ScientificFull timeWork experience placementWorldwide
- ...within the Synthetic Molecule CMC organization at AbbVie is... ...effective communication within scientific teams and senior CMC management... ...Sciences, Biomedical Engineering, Chemical Engineering, or Material... ...related to formulation design Technical awareness in various aspects...ScientificFull timeTemporary workLocal area
- ...analytical sciences organization responsible for CMC analytical activities related to the... ...regulatory documents, laboratory data, technical memos and reports. Proactively advise... ...analytical strategies. Demonstrate scientific excellence in analytical...ScientificFull timeWork experience placementLocal area
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- ...the product development and CMC teams and will have strong collaborations... .... Initiate and/or support scientific initiatives to drive... ..., Chemistry, Chemical Engineering, or related disciplines with... ...influence without authority, drives technical excellence, and inspires...ScientificFull timeTemporary workLocal area
- ...Analytical R&D) is a global analytical scientific organization responsible for all CMC analytical activities related to... ..., demonstrate broad versatile technical expertise. He/she should possess... ...PCS), Process Chemistry, Process Engineering, Drug Product Development (DPD),...ScientificFull timeTemporary workLocal area
- ...strategy across Synthetic Molecules CMC R&D. The candidate will... ...documents, laboratory data, technical memos and reports. The... ...chemists, analytical chemists, engineers, drug product development... ...Experience managing and developing scientific leaders and teams in CMC is...ScientificFull timeWork experience placementLocal areaWorldwide
- ...Accounabilty / Scope: Completes daily responsibilities as assigned by labhead Adherence to EHS safety mandates Qualifications: AS or BS in scientific field (chemistry or biology preferred) Attention to detail is critical Ability to prioritize effectively and multi-task within an...ScientificShift work
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