Duties will vary depending on the specific project but will include developing and maintaining standardized content modules for pharmaceutical documentation. This involves maintaining version control for all documents and ensuring timely reviews and approvals. The role will also include some system design, installation, implementation, integration, startup, validation, and customer support. During onsite validation, employees will periodically be required to troubleshoot and modify electrical and PLC controlled systems. Customer location varies depending on project needs, generally in the Greater Philadelphia, PA area, Raleigh, NC and Northern New Jersey.
Job Responsibilities
- Industrial automation system validation & validation documentation
- PLC and HMI programming on various platforms
- Drives and motion control on various platforms
- Microsoft operating systems, office, and networking
- Electrical design & troubleshooting
- GMP knowledge & experience
General Job Information
TRAVEL OPPORTUNITIES: Up to 30%
SCHEDULE: M-F
OVERTIME OPPORTUNITIES: Occasional
INDUSTRY: Pharmaceutical
HOW TO APPLY: We DO NOT screen candidates through external hiring sites. Please send a copy of your resume and transcripts, along with your video interview availability, to recruiter@mdiadvantage.com. Please mention if you recently met us at an on-campus recruiting event. If we are going to proceed with your application, we will reach out within 2 weeks. Thank you!
