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Automation & Manufacturing Systems Engineer (GMP Production Support) - (JP15234)

New Albany, OH · Biotech/Pharmaceutical
Job Title:   Automation & Manufacturing Systems Engineer (GMP Production Support) - (JP15234)
Location: New Albany, OH. 43054
Employment Type: Contract
Business Unit: Manufacturing Systems Engineering
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 04/14/26
Pay Rate: $34 - $37/hour W2
Notes: Only qualified candidates need apply.  Fully onsite.  Some overtime may be required

3 Key Consulting is hiring an Automation & Manufacturing Systems Engineer (GMP Production Support) for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Job Description:
  • Position involves support of senior staff in the initiation, design, and delivery of projects, particularly for automation related scope.
  • Employ basic engineering skills and practices to gather user requirements and translate them into technical documentation for execution by third party firms.
  • Assist with project definition by performing engineering studies and assessment for automation system installations.
  • Perform field evaluations of existing systems and provide engineering design recommendations.

Why is the Position Open?
Supplement additional workload on team


Top Must Have Skills:
  • 1–2+ years of hands-on experience in a GMP-regulated environment
  • Work In teams, communication
  • Mechanical systems experience

Day to Day Responsibilities:
  • Monitor daily operations of production lines.
  • Assist with troubleshooting downtime related issues, manage line improvements, work through CAPAs and deviations.

Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience

Preferred Qualifications:
  • Previous intern experience is a plus.
  • Experience with automation is a plus.
  • Experience with computer programming, systems, and/or robotics is a plus
  • Experience working in an FDA-regulated environment
  • Familiarity with maintenance management software (e.g., Maximo)
  • Experience with 3D modeling tools such as SolidWorks or similar
  • Strong technical writing skills

Employee Value Proposition:
Opportunity to gain experience working in an FDA and GMP regulated environment.

Red Flags:
  • Inability to meet core job requirements.
  • Poor communication skills.
  • Unable to work OT as needed.
  • Flexibility is required as workload increases.


Interview process:
One on one - Panel interview


We invite qualified candidates to send your resume to0.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
 
 
Regards,
 
3KC Talent Acquisition Team
 
 

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