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AQL Inspector - 2nd shift

Location: Durham, United States
Position Type: Unfixed Term
Job Function: Quality

A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions that detect disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 5,000 team members across 12 sites or subsidiaries, including Salt Lake City based BioFire Diagnostics. We believe in the power of diagnostics and bioMérieux sponsors public health initiatives and partnerships to address antimicrobial resistance, sepsis awareness, food safety, and consumer health across the globe. Come be a part of our mission to help save lives.

 

Position Summary:

The AQL inspector performs Quality Assurance inspection of finished product following specified AQL sample plans. They identify visual defects and check that labeling, bar coding, expiry dates and carton contents for products are compliant. They verify labeling and packaging line setup.

 

The AQL inspector completes inspection documentation in accordance with BMX controlled documentation procedures. They also review labeling and documentation for completeness on the packaging floor. They document any identified non-conformances in accordance with site procedures.

 

Responsibilities:

  • Performs finished product inspection for visual defects, completes inspection documentation and reviews entered inspection data to ensure products meet specifications.
  • Completes AQL sample plan calculation worksheets.
  • Supports labeling and packaging line documentation review on-the-floor for BacT/ALERT products.
  • Reports status of documentation errors to management in a timely manner.
  • Assists with modifications of inspection procedures to assure product quality

 

Studies and Experience:

  • Associate's Degree, or High School Diploma/GED and 5 years of experience working in a FDA regulated, GMP production facility.

 

Skills and Qualifications:

  • Ability to clearly express ideas (verbal and written).
  • Experience working in a FDA regulated, GMP production facility.
  • Knowledge of Good Documentation Practices.
  • Ability to understand and act on verbal and written instuctions, including written product specifications.
  • Strong interpersonal skills and ability to work with all levels of an organization.
  • Capacity to work alone as well as in a team environment.
  • PC skills: proficiency in using Microsoft Office Suite.

 

Joining bioMérieux, is choosing to join an innovative company with a long term vision, committed to the service of public health and carried out with a humanistic corporate culture. Our Group offers numerous possibilities: so come and join the 13,000 bioMérieux team members who already identify with these values!

 

bioMérieux is an Equal Opportunity, Affirmative Action Employer. M/F/Vet/Disability/Sexual Orientation/Gender Identity/GINA.

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