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Now viewing: Digital Engineer
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i-Pharm GxP
Digital Engineer
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Job Description
Digital Engineer at i-Pharm GxP Digital Engineer at i-Pharm GxP in Lebanon, Indiana Posted in about 19 hours ago.
Type:
full-time Digital Plant Engineer - Hybrid - Automation & Process Systems (Contract) Are you an Automation Engineer who excels at bridging functional silos between process engineering, operations, IT, and automation teams? We are seeking a Digital Plant Engineer for a multi-billion-dollar greenfield capital project, constructing highly flexible GMP clinical trial drug substance facilities for a leading global pharmaceutical manufacturer.
Engagement Details Location:
Hybrid in Central Indiana (Minimum 2 weeks a month on-site for the first 6 months; minimum 1 week a month thereafter).
Duration:
2+ years desired.
Scope:
Producing drug substances for small molecules, biologics, and nucleic acid therapies. The Role Join the dots between Business, Technology, and Data architectures for the facility. Embed into Project Automation Teams to understand product manufacturing processes and ensure digital solutions align with facility design and regulatory requirements. Lead data flow mapping activities and contribute to the delivery of site-level data infrastructure (e.g., Aveva PI, Logmate). Bridge process control, automation-MES integration, historian delivery, PAT platform oversight, digital use case scoping, and data integrity compliance. Interact extensively with the central engineering office, Process Engineering, Process Technical Transfer, Enterprise IT, and the end users. What We're Looking For BS in Engineering (or equivalent experience) with 7+ years of experience in API/bulk manufacturing within the Pharmaceutical Industry. Strong automation and OT operations background, specifically in DCS engineering and batch manufacturing. Proven ability to translate process and operational needs into digital requirements. Previous experience in DeltaV Batch DCS and the delivery of large automation projects in the Pharmaceutical Industry. Strong knowledge of GMPs, regulatory requirements, and computer system validation principles.
Preferred:
Previous experience with MES systems and Aveva PI.