Engineer, GMP Production Line Support & Automation - (JP15234)

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.