Jobs / AstraZeneca / Associate Director, Digital & Business Process Strategy

Associate Director, Digital & Business Process Strategy

AstraZeneca
US - Rockville - MD Onsite Information Technology
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About this role

The Associate Director, Digital & Business Process Strategy leads the vision, roadmap, and value delivery of digital products that span PASX, Tulip (MES), data historians, and LIMS within AstraZeneca’s manufacturing network. This role sits in the Digital & Business Process Strategy team and partners with Operations, Quality, Global IT, Data & AI, Supply Chain and Site teams to modernize data flows, improve RightFirstTime, and enable compliant, datadriven decision making from shop floor to enterprise. You will be based in Rockville, MD and report to the Senior Director of Digital & Business Process Strategy.

Key responsibilities 

1. Product vision and roadmap 

  • Define and socialize a compelling product vision linking MES (PASX, Tulip), Historian - CDZ, and LIMS capabilities to business outcomes (yield, cycle time, batch release, deviation reduction) 

  • Build and manage a multirelease roadmap, balancing global platforms with site needs, technical debt, and regulatory priorities. 

  • Maintain a prioritized, valueranked backlog with clear acceptance criteria and Definition of Done. 

2. Stakeholder and value management 

  • Act as the voice of Operations, Quality, and QA/QP in product decisions; translate pain points into epics/features to deliver e2e business process maps and well-defined business requirements  

  • Quantify value through OKRs/KPIs (e.g., batch review time, exception rates, data availability SLAs) and track benefits realization. 

3. Delivery leadership 

  • Lead agile squads (process SMEs, solution architects, data engineers, MES configuration, historians, LIMS specialists, validation) to deliver increments. 

  • Coordinate integration patterns between MES, historians, LIMS, ERP, data platforms, and analytics/AI products. 

  • Ensure robust data models, master data stewardship, and event/transaction standards supporting traceability across systems. 

4. Compliance and validation 

  • Ensure products comply withGxP, 21 CFR Part 11/Annex 11, data integrity (ALCOA+), and site/enterprise validation requirements. 

  • Own validation strategy for changes (CSV/CSA), including risk assessments, test evidence, and audit readiness. 

5. Data and analytics enablement 

  • Enable contextualized data capture and lineage from equipment and MES to historian and LIMS; expose governed data to analytics platforms. 

  • Partner with Data & AI teams on use cases such as realtime deviation detection, golden batch, CPV/Continued Process Verification, and eBR/eBRR optimization. 

6. Operations readiness and lifecycle management 

  • Plan releases, cutovers, and change management across multiple sites; coordinate training and SOP updates. 

  • Own product performance, reliability, and cybersecurity posture; manage incidents, problem remediation, and continuous improvement. 

  • Manage vendor relationships (e.g., Körber, Factory Talk, PASX, Tulip, Historian and LIMS providers) and ensure contract deliverables align to roadmap. 

Required qualifications 

  • Bachelor’s degree in engineering, life sciences, computer science, or related field; advanced degree preferred. 

  • 8+ years in pharma/biotech or highly regulated manufacturing with handson exposure to at least two of the following: PASX (or equivalent MES), process data historians (e.g., PI/AVEVA, IP.21, Ignition), LIMS/ELN. 

  • 3+ years as a Product Owner or equivalent (product management, solution owner) delivering digital capabilities in GxP environments. 

  • Strong understanding of manufacturing and quality processes: recipe management, eBR, batch disposition, deviation/CAPA, CPV, stability, and sample lifecycle. 

  • Demonstrated experience integrating shopfloor systems with enterprise platforms (ERP, QMS) and data/analytics stacks; familiarity with ISA95/ISA88 models and data standards. 

  • Practical knowledge of CSV/CSA, GAMP 5, data integrity, and audit expectations. 

Preferred qualifications 

  • Experience with PASX configuration and content management; knowledge of interface frameworks, EBR review workflows, and exception handling. 

  • Background in OT/IT convergence: OPC UA, MQTT, edge connectivity, timeseries data modeling, and event streaming. 

  • Working knowledge of modern data platforms and analytics (e.g., cloud data lakes, timeseries services, visualization, ML for manufacturing). 

  • Certification in Agile/Scrum (PSPO, CSPO) and/or product management; Lean Six Sigma or equivalent continuous improvement credentials. 

  • Experience operating across multisite/global manufacturing organizations and managing vendor ecosystems. 

Key competencies 

  • Business value orientation converts operational challenges into measurable outcomes and prioritizes accordingly. 

  • Systems thinking understands endtoend data flows from equipment and MES to LIMS/quality and enterprise analytics. 

  • Stakeholder influence: builds alignment across Operations, Quality, IT, and site leadership. 

  • Decision making under compliance: balances speed with validation and data integrity requirements. 

  • Communication and change leadership; simplifies complex topics and drives adoption. 

  • Delivery excellence: strong backlog management, release planning, and risk mitigation. 

The annual base pay for this position ranges from $122K to $184K. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans. 

Date Posted

26-May-2026

Closing Date

08-Jun-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

About AstraZeneca

Global biopharmaceutical company focused on oncology, cardiovascular, renal, and respiratory therapies. Headquartered in Cambridge, UK.

astrazeneca.com

Job Details
LocationUS - Rockville - MD
Work typeOnsite
DepartmentInformation Technology
SeniorityDirector
CountryUnited States
About the company
AstraZeneca
Global biopharmaceutical company focused on oncology, cardiovascular, renal, and respiratory therapies. Headquartered in Cambridge, UK.
View all 1556 open jobs at AstraZeneca
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