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AstraZeneca

Associate Director, Digital & Business Process Strategy

Discovered
AstraZeneca
US - Rockville - MDFull timePosted 13 days ago (Jul 31, 2026)

About the role

The Associate Director, Digital & Business Process Strategy leads the vision, roadmap, and value delivery of digital products that span PAS ‑ X , 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   Right ‑ First ‑ Time , and enable compliant,   data ‑ driven   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.

1. Product vision and roadmap

• Define and socialize a compelling product vision linking MES (PAS ‑ X , Tulip ), Historian   - CDZ , and LIMS capabilities to business outcomes (yield, cycle time, batch release, deviation reduction)   • Build and manage a   multi ‑ release   roadmap, balancing global platforms with site needs, technical debt, and regulatory priorities.   • Maintain a prioritized,   value ‑ ranked   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 with   GxP , 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   real ‑ time   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,   PAS ‑ X,   Tulip, H istorian 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   hands ‑ on   exposure to at least two of the following: PAS ‑ X (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   shop ‑ floor   systems with enterprise platforms (ERP, QMS) and data/analytics stacks; familiarity with ISA ‑ 95/ISA ‑ 88 models and data standards.   • Practical knowledge of CSV/CSA, GAMP 5, data integrity, and audit expectations.

Preferred qualifications

• Experience with PAS ‑ X configuration and content management; knowledge of interface frameworks, EBR review workflows, and exception handling.   • Background in OT/IT convergence: OPC UA, MQTT, edge connectivity,   time ‑ series   data modeling, and event streaming.   • Working knowledge of modern data platforms and analytics (e.g., cloud data lakes,   time ‑ series   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   multi ‑ site /global manufacturing organizations and managing vendor ecosystems.

Key competencies

• Business value   orientation   converts operational challenges into measurable outcomes and prioritizes accordingly.   • Systems   thinking   understands   end ‑ to ‑ end   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

31-Jul-2026

Closing Date

10-Aug-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.

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This role was discovered from a public careers page. Applications are handled by the hiring team at AstraZeneca.

Attribution: sourced from AstraZeneca's public Workday board.

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