Assembler (Parapak)

Meridian BioscienceCincinnati, OH
66d$17

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) strongly preferred.
  • 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.

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.
  • 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.

Benefits

  • Pay Rate: $17.00, non-negotiable
  • Hours: 5:00am-1:30pm, Monday- Friday, with a Saturday rotation

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What This Job Offers

Job Type

Full-time

Industry

Professional, Scientific, and Technical Services

Education Level

High school or GED

Number of Employees

501-1,000 employees

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