Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.

Responsible for the final inspection of all assigned product lines and associated materials for defects or deviations from specifications in accordance with current Standard Operating Procedures and Quality System Regulations. Report to management any noted defects or failures during the inspection and testing process.  Verify correct components and labeling were used in assembly.

Tasks/Duties/Responsibilities:

• Read parts lists.
• Inspect, test, or measure materials or products being produced.
• Accept or reject finished items.
• Segregate products and materials that fail to meet specifications.
• Discuss inspection results with those responsible for products.

• Approves finished products by confirming specifications; initiating deviation reports when failures are observed.

• Keeps inspection equipment operating by following operating instructions; calling for repairs.

• Maintain complete, thorough, up-to-date documentation and filing of completed inspection reports and test data.
• Maintains safe and healthy work environment by following standards and procedures; complying with legal regulations.

Other duties as assigned:

• Ability to read, understand and follow all company Standard Operating Procedures (SOPs)
• Must be able to use specialized tools and machinery when testing products.

• Must understand parts lists, ensuring that products and parts meet quality standards and guidelines.
• Must be able to follow chemical safe handling procedures.

• Proficient in utilizing the MS Office Suite (Word, Excel, PowerPoint and Outlook)
• Must be able to wear personal protective equipment (latex or nitrile gloves, safety glasses/face shields, lab coat, etc.).
• Must be able to adhere to applicable bio-safety practices when on the manufacturing floor.
• Ability to work on a PC including repetitive use of a keyboard and mouse for long periods throughout the course of the workday.
• Must be able to analyze, concentrate, and solve complex issues throughout the workday.

Minimum Education or Equivalent Experience Required/Preferred:

• High School Diploma or general education degree (GED) required.
• One year of experience in Quality Control with electro-mechanical background within an FDA-regulated manufacturing, or laboratory environment is preferred. Clerical/inspection background is preferred.

Competencies Required or preferred:

• Must be able to perform basic mathematical calculations (addition, subtraction).
• Must be a self-starter, detail oriented, organized and be able to perform under pressure in a fast-paced environment.
• Excellent interpersonal, organizational, written and oral communications skills.
• Strong attention to detail.
• Must able to work independently as well as collaboratively in a team setting with peers and colleagues in a cross functional setting.
• Ability to walk up and down several flights of stairs throughout the workday in a multi-location facility.

Required Travel %:

• Not anticipated. However, must be able to travel by car/air to other MBI locations and/or supplier locations as needed

*We are proud to be an EEO/AA employer Minority/Female/Disability/Veteran. We maintain a drug-free workplace and perform pre-employment substance abuse testing. (USA Only)*