Position Details

Salary $64K – $184K USD / year

Type Full-Time

Experience mid

Exp. Years Not specified

Education Not specified

Category Engineering (Non-Software)

About this role

Support and develop manufacturing execution systems at Lilly's Indianapolis site, focusing on validation, configuration, and digital transformation to enhance manufacturing efficiency and compliance.

Key Responsibilities

Support MES platform
Validate system configurations
Drive digital transformation
Collaborate with manufacturing teams
Ensure compliance and validation

Technical Overview

Involves MES platforms like PMX and PharmaSuite, system validation, configuration, and supporting digital transformation efforts in pharmaceutical manufacturing.

Ideal Candidate

The ideal candidate is a mid-level MES Systems Engineer with experience in manufacturing execution systems, validation, and digital transformation projects within the pharmaceutical industry. They are collaborative, detail-oriented, and capable of supporting complex MES platforms.

Must-Have Skills

MESSystem DesignValidationConfigurationManufacturing Processes

Nice-to-Have Skills

PharmaSuiteDigital TransformationElectronic Master Batch RecordsAutomation

Tools & Platforms

MESPMXPharmaSuite

Required Skills

MESManufacturing Execution SystemsSystem DesignValidationConfigurationElectronic Master Batch RecordsDigital TransformationPharmaSuite

Hard Skills

Manufacturing Execution SystemsMESPMXPharmaSuiteSystem DesignValidationConfigurationElectronic Master Batch RecordsAutomationDigital Transformation

Soft Skills

CollaborationProblem-solvingCommunicationAdaptabilityTeamwork

Industry & Role

Industry Healthcare IT

Job Function MES system engineering supporting manufacturing operations and digital initiatives

Keywords for Your Resume

MESManufacturing Execution SystemsSystem EngineerValidationConfigurationElectronic Master Batch RecordsDigital TransformationPharmaSuiteSupportManufacturing ProcessesSystem Design

Deal Breakers

Lack of MES experience, No experience with validation or system design, Unfamiliar with pharmaceutical manufacturing processes, Inability to support digital transformation

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