Position Details
About this role
This role involves providing automation engineering support for pharmaceutical manufacturing at the Rahway, NJ facility, ensuring compliance, system validation, and operational support for clinical supply processes.
Key Responsibilities
- Maintain automation systems in a validated state
- Support non-sterile clinical manufacturing
- Implement automation solutions and documentation
- Lead automation change control and investigations
- Represent automation in capital projects
Technical Overview
The technical environment includes automation systems, OT/IT architecture, data analytics, cybersecurity, and validation processes within a cGMP pharmaceutical manufacturing setting.
Ideal Candidate
The ideal candidate is a senior automation engineer with extensive experience in pharmaceutical manufacturing, cGMP compliance, and automation lifecycle management. They should possess strong troubleshooting and data integrity skills, with a background supporting clinical supply manufacturing environments.
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 experience with cGMP automation systems, No pharmaceutical manufacturing background, Unwillingness to work onsite in Rahway, NJ
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