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Product Quality Assurance AssociateMeridian Bioscience International Limited • Cincinnati, Ohio, United States
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Product Quality Assurance Associate

Meridian Bioscience International Limited
  • US
    Cincinnati, Ohio, United States
  • US
    Cincinnati, Ohio, United States
Postuler Maintenant

À propos

About Meridian 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.
Job Summary Responsible for the initiation and completion of lot logs, adding C of As to the indicated location, review of production paperwork as required. Performs all tasks in compliance to the company’s quality system requirements.
Key Duties Tasks/Duties/Responsibilities:
Initiate and complete Lot Release logs in Master Control
Ensure all Lot Release records are appropriately stored, maintained and retrievable.
Ensure all good documentation practices are always adhered to.
Maintain complete, thorough and timely documentation.
Interact cooperatively with team members at all levels and receive instruction well from all senior staff
Participate in the review of production records, work instructions or other quality records to ensure products made available for distribution meet predetermined formulation, inspection requirements and testing requirements
Other duties as assigned
Other Duties / Physical Requirements
Physical
Ability to walk up and down several flights of stairs throughout the workday in a multi-location facility.
Ability to sit for long periods of time, bend, reach and twist through the course of the workday.
Other
Must be able to adhere to applicable safety practices when on the manufacturing floor or in laboratories.
Ability to analyze, concentrate and review paperwork for long periods of time in an open work environment.
Ability to work on a computer including repetitive use of a keyboard and mouse for long periods throughout the course of the workday.
Qualifications Minimum Education or Equivalent Experience Required/Preferred
Bachelor’s degree in Biology, Biochemistry or Microbiology is preferred or equivalent experience in a related industry.
Previous experience in document review and/or manufacture of diagnostics kits is preferred, but not required.
Competencies Required or Preferred
Ability to read, understand and follow all company SOPs and Guidelines
Computer proficiency (Word and Excel)
Excellent interpersonal, organizational, written and oral communication skills.
Must be well organized and can meet strict deadlines and perform under pressure in a fast-paced environment
Must be able to work independently as well as collaboratively in a team setting with peers and other departments in a cross functional setting
Must be a self-starter, detail oriented and able to prioritize and balance both workload and timelines
Required Travel %
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  • Cincinnati, Ohio, United States

Compétences linguistiques

  • English
Avis aux utilisateurs

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