Data Management Lead

Xyntek Inc.; Indianapolis (IN); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading company in the pharmaceutical sector seeks a Data Management Lead in Indianapolis to oversee data architecture projects. The ideal candidate should possess over 8 years of data management experience, especially in API manufacturing, and have expertise in Aveva PI. Responsibilities include collaborating across teams to ensure robust data management solutions, leading projects, and supporting system integration efforts.

Qualifications

• 8+ years working data management experience in the Pharmaceutical Industry.
• Experience in Aveva PI installation, configuration, and integration.
• Strong knowledge of GMPs, regulatory requirements, and computer system validation principles.

Responsibilities

• Manage data management projects and collaborate with various teams.
• Develop data management requirement specification documents.
• Communicate progress, issues, and needs to the program manager.

Skills

Data Management

Teamwork

Communication

Process Templates

Tools

Aveva PI

KepserverEx

MQTT

DeltaV

Rockwell

Job description

Indianapolis, United States | Posted on 05/27/2025

Catalyx specializes in the science of operational processes. With afootprint across North America and Europe, the company carefullyautomates and services R&D, production, packaging, and deliveryprocesses—globally—with a sophisticated blend of products,technologies, and lifecycle services. The company was formed in 2022after CXV Global (Crest Solutions, Xyntek, and VistaLink) and PanaceaTechnologies joined forces. For over three decades, Catalyx’spartnership-based culture has helped organizations inproduction-intense, highly regulated industries optimize theiroperational efficiency, performance, and safety. To learn more aboutthe company's experience and comprehensive suite of capabilitiesand solutions, visit www.catalyx.ai .

Job Description

The Data Management Lead will be responsible for identifyingrequired 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 Integritychampion, Engineering Tech Centre and Technical services groups to identifyrequired data architectures and data models

Participate in overall data architecture design

Development of data management requirement specificationdocuments.

Develop scope and delivery model for the data managementprojects

Management of the data management projects

Management of the System Integrators executing the datamanagement projects.

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

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

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

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

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

Communicate progress, issues, and needs to the Foundryautomation program manager

Responding to system integrator technical queries

Support the development of testing strategies

Requirements

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

AvevaPI installation and configuration experience in the following areas: PI siteinfrastructure, data archive, and interfaces

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

PIVision

Experiencewith integration of Aveva Pi with automation systems (Preferable Emerson DeltaVand Rockwell)

Experiencewith integration of Avena PI with OT systems e.g. KepserverEx platform and MQTTmessage broker e.g. HiveMQ

PreviousPharmaceutical Automation Large Project/Program experience/expertise

Exceptionalteamwork abilities

Strongknowledge of GMP’s, regulatory requirements and computer system validationprinciples

Excellentwritten and verbal communication skills for both technical and non-technicalaudiences

Strongknowledge of GMP’s, regulatory requirements and computer system validationprinciples

Excellentwritten and verbal communication skills for both technical and non-technicalaudiences