NEOGEN CORP. 1st Shift QC Technician I in Lansing, MI

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Come Be Part of a Mission that Matters!

Prepares and tests validation procedures/protocols to ensure the product is manufactured in accordance with appropriate regulatory agency validation requirements, internal company standards and current industry practices. Compiles and analyzes validation data, prepares reports and makes recommendations for changes and/or improvements. May also investigate and troubleshoot problems and determine solutions. Maintains validation documentation and files.

Perform routine chemical, immunochemical, biological or microbiological assays on manufactured diagnostic products to determine compliance with specified performance standards.

Hours: Monday - Thursday 6:00am - 4:30pm

Essential Duties and Responsibilities:

  • Perform routine chemical, immunochemical, biological or microbiological assays in accordance to appropriate Standard Assays Procedure (SAP) or Standard Operating Procedure (SOP).
  • Adhere to good lab practices (GLP) guidelines in daily activities.
  • Adhere to International Organization for Standardization (ISO) guidelines in daily activities.
  • Assist in the development of new QC procedures.

Education and/or Experience: Minimum Associates degree in science-related field OR High School diploma with some college science and 1 year QC Lab Tech experience.

WHO IS NEOGEN:

From farm to fork, we offer solutions to enhance the quality, quantity and safety of the global food supply. Our food safety diagnostics are used within farming operations to the production facilities of most of the world’s best-known food companies. Neogen’s solutions are critical to the health and well-being of our customers’ operations – and in turn their consumers. What we do matters!

Neogen’s culture combines stability with a deep believe in providing professional and personal growth. Our Pillars of Trust – the principles which guide our everyday decision—making, include Openness, Honesty, Credibility, Respect, and Service. It’s the belief in these characteristics that provide a consistent, happy and healthy work environment for our employees.


Prepares and tests validation procedures/protocols to ensure the product is manufactured in accordance with appropriate regulatory agency validation requirements, internal company standards and current industry practices. Compiles and analyzes validation data, prepares reports and makes recommendations for changes and/or improvements. May also investigate and troubleshoot problems and determine solutions. Maintains validation documentation and files. Perform routine chemical, immunochemical, biological or microbiological assays on manufactured diagnostic products to determine compliance with specified performance standards. Hours: Monday - Thursday 6:00 am - 4:30 pm. Essential Duties and Responsibilities:Perform routine chemical, immunochemical, biological or microbiological assays in accordance to appropriate Standard Assays Procedure (SAP) or Standard Operating Procedure (SOP). Adhere to good lab practices (GLP) guidelines in daily activities. Adhere to International Organization for Standardization (ISO) guidelines in daily activities. Assist in the development of new QC procedures. Education and/or Experience: Minimum Associates degree in science-related field OR High School diploma with some college science and 1 year QC Lab Tech experience.
search terms: Technician+QC
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