Job Title: Engineer, GMP Production Line Support & Automation - (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
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.