Engineer, GMP Production Line Support & Automation - (JP15234
Listed on 2026-08-12
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Engineering
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.
- Monitor daily operations of production lines.
- Assist with troubleshooting downtime related issues, manage line improvements, work through CAPAs and deviations.
- 1–2+ years of hands‑on experience in a GMP-regulated environment.
- Work in teams, communication.
- Mechanical systems experience.
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 internship 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 Solid Works or similar.
- Strong technical writing skills.
Opportunity to gain experience working in an FDA and GMP regulated environment.
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