Product Quality Assurance Associate

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, redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals who 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 initiation and completion of lot logs, adding C of As to the indicated location, reviewing production paperwork as required. Performs all tasks in compliance with the company’s quality system requirements.

• Initiate and complete Lot Release logs in Master Control
• Ensure all Lot Release records are appropriately stored, maintained and retrievable.
• Ensure compliance with Good Documentation Practices.
• Maintain complete, thorough and timely documentation.
• Interact cooperatively with team members at all levels and receive instruction well from senior staff.
• Participate in review of production records, work instructions or other quality records to ensure products meet predetermined formulation, inspection and testing requirements.
• Other duties as assigned.

• Physical:
  • Walk up and down several flights of stairs throughout the workday in a multi‑location facility.
  • Sit for long periods of time, bend, reach and twist during the workday.
• Other:
  • Adhere to applicable safety practices when on the manufacturing floor or in laboratories.
  • Analyze, concentrate and review paperwork for long periods in an open work environment.
  • Work on a computer, including repetitive use of keyboard and mouse for long periods.

• Bachelor’s degree in Biology, Biochemistry or Microbiology preferred, or equivalent experience in a related industry.
• Previous experience in document review and/or manufacture of diagnostic kits preferred.

• Read, understand and follow company SOPs and Guidelines.
• Computer proficiency (Word and Excel).
• Excellent interpersonal, organizational, written and oral communication skills.
• Self‑organized, meet strict deadlines and perform under pressure in a fast‑paced environment.
• Work independently as well as collaboratively in teams and with other departments in cross‑functional settings.
• Self‑starter, detail oriented and able to prioritize and balance workload and timelines.