Quality System Associate

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Job Details

Where: Iowa—Des Moines, USA

Type of Contract: Regular Full-Time; Subject: Nursing/Healthcare

Request ID: 513811

Primary Responsibilities

  • Review donor record files every day.

  • Conduct quality control reviews on equipment on a daily, weekly, monthly, semi-annual, and annual basis.

  • Evaluate equipment incident logs once a week.

  • Shipment verification and sample release.

  • Stage plasma in preparation for shipping.

  • Examining and releasing new supplies.

  •  Take part in and contribute to the Quality Assurance team by attending meetings.

  • Help the Center Quality Manager make sure cGMP guidelines are being followed.

  • Help the Center Quality Manager make sure that regulations are satisfied and SOPs are followed.

  • Examines the paperwork pertaining to inappropriate test findings and the handling of the related units.

  • The following tasks may occasionally need to be completed by the Quality Associate in the absence of the Center Quality Manager:

  • Completes all tasks related to product release.

  •  Keeps track of, looks into, and does root cause analysis for deviations and customer complaints, particularly when they have to do with donor safety and product quality

  • Equipment records and DMS data are reviewed, if necessary, to authorize the usage of out-of-service machinery.

  • Evaluation and authorization of postponed donor reintegration initiatives.

  • Evaluate the lookback data. Evaluate the waste shipment.

  • Before using any supplies, start an inquiry and report those that don't match quality standards and criteria.


Primary requirements

Extra Duties

possesses and upholds certification in the field of donor processing.

Instruction

GED or a high school diploma. if necessary, obtains state certificates or licenses.

Experience

Usually doesn't require any prior experience in the field. 

 



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