Position Details
About this role
This role involves supervising automation hardware and control systems supporting GMP manufacturing at Lilly’s new facility, ensuring compliance, and leading project and site support activities.
Key Responsibilities
- Supervise automation hardware and control systems
- Support GMP manufacturing operations
- Lead project delivery and startup activities
- Manage site support functions
- Ensure regulatory compliance
Technical Overview
Focus on automation hardware, control systems, GMP processes, and manufacturing support with project management and leadership in a pharmaceutical environment.
Ideal Candidate
The ideal candidate is a mid-level engineering professional with experience supervising automation hardware and control systems in GMP manufacturing environments. They possess strong leadership skills and a background in pharmaceutical or biotech production processes.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of GMP manufacturing experience, No supervision experience in automation hardware, Unfamiliarity with pharmaceutical regulations
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