The Data Management Lead will be responsible for identifying required data architectures/data models and managing the data projects (e.g. Historian Project, Alarm Management etc.) within the overall Foundry program.

Role Responsibilities:

Collaborate with the Lilly site team, Data Integrity champion, Engineering Tech Centre and Technical services groups to identify required data architectures and data models

Participate in overall data architecture design

Development of data management requirement specification documents.

Develop scope and delivery model for the data management projects

Management of the data management projects

Management of the System Integrators executing the data management projects.

Work with Lilly technical departments to develop process and asset templates in support of data models

Identify any equipment specific data that needs to be captured for maintenance, operations etc.

Work closely with the Foundry automation technical office on data management in relation to information security

Collaborate with the Automation Project teams to ensure data management solutions are aligned with project system architecture and schedule

Collaborate with the Digital/MES work-stream leads to align the data management solutions

Communicate progress, issues, and needs to the Foundry automation program manager

Responding to system integrator technical queries

Support the development of testing strategies

Requirements

BS Engineering (or equivalent experience)

8+ years working data management experience in the Pharmaceutical Industry (preferable in API/bulk manufacturing)

Aveva PI installation and configuration experience in the following areas: PI site infrastructure, data archive, and interfaces

PI Asset Framework: Elements, Analyses, Event Frames, PI Notifications

PI Vision

Experience with integration of Aveva Pi with automation systems (Preferable Emerson DeltaV and Rockwell)

Experience with integration of Avena PI with OT systems e.g. KepserverEx platform and MQTT message broker e.g. HiveMQ

Logmate or alternative alarm management system experience

Previous Pharmaceutical Automation Large Project/Program experience/expertise

Exceptional teamwork abilities

Strong knowledge of GMP’s, regulatory requirements and computer system validation principles

Excellent written and verbal communication skills for both technical and non-technical audiences

Strong knowledge of GMP’s, regulatory requirements and computer system validation principles

Excellent written and verbal communication skills for both technical and non-technical audiences