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.