Lansing Hiring Event - Machine Operators, Quality Techs and Lab Support

Neogen Corporation•Lansing, MI

13d•Onsite

About The Position

Neogen Corporation is hosting a hiring event for open Machine Operator (all shifts), Quality Technician, and other laboratory support positions. The company fosters a culture of innovation, collaboration, and continuous improvement, offering competitive compensation and benefits, as well as opportunities for professional growth and development. The mission is to protect and enhance global food and animal safety. These roles follow an onsite model to accommodate business needs while maintaining team collaboration.

Requirements

High school education; or up to one-month related experience or training; or equivalent combination of education and experience.
Minimum of Associate's degree in a science-related field and 1-2 years of relevant microbiology laboratory experience.
OR High School diploma with some college coursework in microbiology or a closely related science field or 3 years of relevant microbiology laboratory technician experience, preferably in a quality control setting.
OR Bachelor's degree in Microbiology or a closely related science field with experience in microbiology is highly preferred.
Ability to read and interpret documents such as safety rules, work instructions, Standard Operating Procedures, and other procedural documents in English, particularly those related to microbiological testing.
Must be able to read computer screens in English, including software used for microbiological data analysis.
Ability to write routine reports and correspondence, including detailed microbiological test reports, and to speak effectively in front of team members and in general group meetings.
Ability to communicate (orally or written) clearly and informatively; edits work for spelling and grammar; presents numerical data effectively, especially microbiological counts and trends; able to read and interpret written information, including microbiological SOPs and regulatory guidelines.
Ability to perform routine, college-level mathematical operations, including statistical functions relevant to microbiological data analysis (e.g., CFU calculations, growth curves).
Solid knowledge of computers and operating systems, including software used for data acquisition and analysis in a microbiology lab.
Ability to effectively communicate electronically.
Knowledge and experience with Microsoft Office Suite (Word, Excel, PowerPoint), with proficiency in using Excel for data analysis and charting of microbiological results.
College education – either graduated or actively pursuing a degree in Protein Chemistry, Chemistry, Biochemistry, or a related field.
Minimum of 1 year related work experience or hands-on college laboratory experience.

Nice To Haves

A minimum tenure of 1 year in the Machine Operator I position is required to be met before consideration for promotion to the next position level: Machine Operator II.

Responsibilities

Operates machinery in a clean environment used in the food safety industry according to Standard Operating Procedures ensuring accuracy and quality throughout the processes.
Uses automated equipment to manufacture, assemble, or move parts/kits/products.
Inspects parts/kits/products to ensure accuracy.
May work at different stations to ensure accuracy.
Maintains equipment and facilities.
Responsible for equipment preventative maintenance of specialized and advanced equipment.
Perform tasks according to the appropriate Standard Manufacturing Procedure (SMP) or Standard Operating Procedure (SOP).
Follow International Organization for Standardization (ISO) guidelines in the manufacture of all reagents.
Use good manufacturing procedures (GMP) and good documentation practices (GDP) in the manufacture of all reagents.
Participate in troubleshooting efforts pertaining to product failures.
Participate in product/process improvement of current products or processes.
Maintains the general cleanliness and organization of work areas using lean processes and 5S.
Operation, maintenance, and calibration of basic equipment necessary to perform job functions.
Adheres to any and all safety rules and regulations, including personal protective equipment, proper use of equipment, proper disposal of any and all materials etc.
Plans and executes necessary preparatory processes for scheduled manufacturing duties in advance.
Participates in the transfer of products from R&D and/or Manufacturability Support to Manufacturing.
Proposes document updates and improvements.
Perform repetitive tasks for extended periods of time, while maintaining attention to detail.
Continually maintains and monitors machine to ensure it functions properly.
Aids in Supply Management.
Assist in physical inventories as required.
Perform other duties as assigned by your supervisor and/or manager.
Comply with and promote all corporate handbook policies.
Comply with, promote, and strive to achieve all corporate and departmental goals.
Comply with, promote, and strive to achieve all productivity, quality, and behavior expectations.
Perform routine and complex assays with a microbiology focus in accordance with appropriate Standard Test Procedures (STPs) or Standard Operating Procedures (SOPs).
These assays may include, but are not limited to, microbial enumeration, identification, sterility testing, and environmental monitoring.
Perform routine chemical, immunochemical, and/or biological assays as needed.
Adhere to Good Laboratory Practices (GLP) guidelines in daily activities, with a strong emphasis on quality testing.
Adhere to International Organization for Standardization (ISO) guidelines in daily activities, with a focus on quality standards.
Assist in the development of new QC procedures, with a strong emphasis on testing and product release.
Help with special projects assigned by Lab Manager, often involving investigations or method development.
Perform equipment qualification, ensuring the suitability of equipment for relevant testing.
Participate in brainstorming sessions to streamline routine activities and troubleshoot manufacturing and QC issues, particularly those involving contamination or control.
Meet individual and departmental goals and objectives, with a focus on maintaining high standards.
Formulate chemical reagents from stock following Standard Manufacturing Procedures (SMPs) and Standard Operating Procedures (SOPs).
Conduct chemical reactions for reagent development under appropriate SOPs/SMPs.
Manufacture reagents in compliance with ISO guidelines and Good Manufacturing Practices (GMP).
Participate in validation and verification procedures related to reagent manufacturing.
Assist in product and process improvements for current products.
Help maintain raw material inventory alongside Supervisor and Manager.
Perform in-process quality testing and final product release testing per documented procedures.
Support other manufacturing activities and projects as assigned.