Manufacturing Engineer
Quick Summary
Assist in updating and generating new Manufacturing, Quality and Maintenance process documentation and data systems.
Assist in updating and generating new Manufacturing, Quality and Maintenance process documentation and data systems.
It's fun to work in a company where people truly believe in what they are doing!
This Manufacturing Engineer will be required to routinely partner with cross-functional teams to support the generation and maintenance of process documentation. They will actively participate in equipment and process qualifications and ongoing quality system audits.
Responsibilities
~1 min read- →Assist in updating and generating new Manufacturing, Quality and Maintenance process documentation and data systems.
- →Revise Standard Operation and Manufacturing Procedures to capture all necessary process, product, and regulatory requirements
- →Assist in developing and managing engineering changes
- →Subject Matter Expert on the manufacturing processes and flow
- →Identify and lead manufacturing improvements and cost reduction projects
- →Perform troubleshooting on new and existing process problems
- →Assist with developing and participating in training for manufacturing personnel
- →Lead CAPA related efforts for the technology platform
- →Primary owner for developing and managing engineering changes
- →Participates in capital requisition proposals and projects
- →Maintains process maps and value stream maps
- →Coordinates with Process Support and R&D as a team member for new technology transfer and development of new technology
- →Assists with complaint investigations and resolution
- →Assists with developing rework protocols where appropriate
- →Participates in maintaining appropriate work environmental conditions and recommends facilities modifications where appropriate
- →Other Duties as assigned.
Requirements
~1 min read- Education and/or Experience: Bachelor’s degree in related field preferred (Industrial Engineering, Biochemistry, Chemistry, Chemical Engineering, etc.) Relevant associate’s degree and greater than five years relevant work experience, or no education and greater than ten years relevant work experience. Preferred experience in the following areas:
- Manufacturing diagnostic testing products/assays
- Sample extraction/testing
- Laboratory experience including Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP)
- Biochemical processes including enzyme-substrate and antibody interactions
- Advanced data analysis utilizing statistical software such as Minitab or Microsoft Excel
- Experimental design, process analysis and LEAN Six Sigma
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
From inside the farm gate to our dinner plates, Neogen protects the world’s food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there — and you can be too.
Location & Eligibility
Listing Details
- Posted
- October 1, 2026
- First seen
- October 2, 2026
- Last seen
- October 2, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 51%
- Scored at
- October 2, 2026
Signal breakdown
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