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.
Essential Duties and Responsibilities
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
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Other Duties as assigned.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
Education and Experience
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
Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to see, talk and hear. The employee is frequently required to stand, walk and sit, for prolonged periods of time. The employee is required to use hands to handle or feel; reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close visual acuity (with or without corrective devices), depth perception and color vision.
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.
Come Be Part Of A Mission that Matters!
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.