Assembler

Meridian BioscienceCincinnati, OH
Onsite

About The Position

The Assembler position requires the employee to learn how to safely assemble, manufacture, and package regulated medical devices and kits in a performance driven environment under the supervision of higher-level operators / Supervisors / Managers. The employee will work to understand and meet all quality standards and adhere to all cGMP standards.

Requirements

  • High School Diploma or general education degree (GED) required.
  • Prior manufacturing and/or assembly experience preferred.
  • Prior experience in an FDA regulated production environment preferred.
  • Learn and retain good documentation practices.
  • Computer literacy / skills required (e-mail and Windows).
  • Must have basic math skills and be able to perform step by step arithmetic calculations.
  • Must show initiative, have critical attention to detail, and be organized.
  • Develop interpersonal, organizational, written, comprehension, and oral communications skills.
  • Ability to maintain regular attendance and punctuality requirements.
  • Must be able to work overtime and weekends to support production efforts as needed.
  • Develop problem solving and troubleshooting skills.

Nice To Haves

  • Prior manufacturing and/or assembly experience preferred.
  • Prior experience in an FDA regulated production environment preferred.

Responsibilities

  • Maintain a safe work environment by complying with all safety and environmental policies including the use of PPE.
  • Expand upon limited knowledge of departmental operations to understand the equipment and processes.
  • Perform manual and automated assembly/packaging of commercial diagnostic products and kits.
  • Read, understand, and comply with current Good Manufacturing Practices and Standard Operating Procedures.
  • Learn to operate and maintain automated production equipment with direct supervision of a trained operator or higher.
  • Complete daily documentation required for production procedures and supplemental documentation as needed.
  • Audit own paperwork for corrections, missing, and/or incomplete information ensuring that it is neat, accurate, and legible.
  • Comply with all OSHA, FDA, ISO, Quality system, Company and departmental requirements.
  • Learn to perform calibrations and routine process monitoring as needed.
  • Conduct in process sampling and/or inspections and document per procedure.
  • Monitor inventory for the purpose of fulfilling daily production needs.
  • Identify and communicate any / all abnormal components and deviating events to the Group Leader/Supervisor/Manager.
  • Learn to use necessary computer programs for the required job tasks.
  • Demonstrate willingness to work with other departments and employees as required and accept instruction from higher level positions.
  • Operator or higher-level employee attention is required at this level.
  • Other duties as required.
  • Must be able to demonstrate/ be competent in multiple skills in 2 departments, listed within the Job Specific responsibilities above, through cross-training over several departments as instructed by management.
  • When in Para Pak Learn how to identify abnormal and out of specification components.
  • Learn how to work all stations of the bagger.
  • Learn how to catch, inspect, and package reagents and complete final case packaging.
  • Learn how to label inner and outer cases.
  • Learn how to identify labels utilizing the correct documentation.
  • Learn how to complete the label reconciliation portion per the respective documentation.
  • Learn to read and understand the Parts List used for every order.
  • Learn to read and understand all applicable SP and EP documents and be able to reference these documents when necessary.
  • Learn how to run the Macro Con labeling machine.
  • When in Rixan Production Learn how to and become proficient in machine setup, machine operation, card inspection, and preventative maintenance.
  • When in Spotting/Blocking Learn and become proficient in the routine tasks of pushing, catching, quality operations, and cleaning.
  • Contribute to the machine setup.
  • When operating the Lyophilizers to Vacuum Dry Learn how to clean and unload a lyophilizer.
  • When operating the Campbell Wrapper/Bosch Poucher Learn how to set up the assets.
  • Learn how to inspect packages per the respective procedures
  • Learn how to perform Leak Testing per the respective procedure
  • When operating the IDS Robotic Cell Learn to inspect strips for acceptable/unacceptable material
  • Learn how to load strips onto the assembly dial
  • When completing manual assembly Learn to inspect strips for acceptable/unacceptable material
  • Learn to assemble strips into the appropriate device
  • Learn to inspect devices for acceptable/unacceptable material
  • When in Plate Coating Learn how to operate, maintain and clean micro well plate coating and packaging room and equipment
  • Learn how to produce, package and label coated microwell plates
  • Learn how to set up/assemble microwell plates for production runs
  • Learn how to set up sealer for coated micro well plates
  • Learn how to set up balances
  • Learn how to calibrate and operate single and multichannel pipettes
  • When in Dispensing. Learn how to set up manual and automated dispensers
  • Learn how to manually label and crimp
  • Learn how to tip, stopper, and cap vials
  • Learn how to setup, operate, and be proficient on Accraply Labelling System
  • Learn how to calibrate and operate balances
  • Learn how to setup and monitor clean room
  • Learn how to properly gown for dispensing clean room
  • When in FID Plate Production Learn how to setup, dispense, punch, inspect, and cleanup.
  • Learn how to assemble FID plates into the final packaging.
  • Learn how to calibrate and operate single
  • When in Kit Assembly Learn how to initiate and complete KPR’s.
  • Learn how to initiate and complete label requests.
  • Learn how set up and calibrate bench top scale.
  • Learn to assemble and perform functions including but limited to pre-assembly stuffing of components, labeling of kit boxes, and weighing kits per the respective production procedures.
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