Manufacturing Engineer

Neogen; Lansing (MI); On-site; USD 70,000 - 100,000; Full time

Job summary

Neogen is seeking a Manufacturing Engineer in Lansing, MI to partner with cross-functional teams to develop, update and manage manufacturing, quality and maintenance process documentation. The role drives CAPA, engineering changes and continuous improvement initiatives across the production floor.

The candidate will contribute to process qualification, data analysis, and LEAN Six Sigma projects, while ensuring GMP/GLP alignment and safe, efficient operations in a fast-paced lab environment.

Qualifications

• Bachelor’s degree in Industrial Engineering, Biochemistry, Chemistry, or Chemical Engineering preferred.
• Relevant associate’s degree with >5 years relevant work experience.
• Experience with GLP and GMP in a manufacturing setting.
• Proficiency in data analysis using statistical software (e.g., Minitab) and Excel.

Responsibilities

• Update and generate Manufacturing, Quality and Maintenance process documentation.
• Revise SOPs to capture all process, product, and regulatory requirements.
• Lead engineering changes and CAPA for the technology platform.
• Identify and lead manufacturing improvements and cost-reduction projects.
• Collaborate with Process Support and R&D on technology transfer and development.

Skills

Process optimization

Cross-functional teamwork

LEAN Six Sigma

Data analysis

Troubleshooting

Documentation

Education

Bachelor’s degree in related field

Associate degree + 5+ years experience

Tools

Minitab

Microsoft Excel

Job description

## Manufacturing EngineerApply: Lansing, MI: Full time: Posted Yesterday: REQ-10779It'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* 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.