QC Inspector - 1st Shift

Innovative Health LLC

Scottsdale (AZ)

On-site

Full time

14 days+

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Job summary

A regulated medical device firm in Arizona is looking for a Quality Inspector to perform critical inspections and testing of components and devices. The role involves documenting results, ensuring compliance with established procedures, and supporting material handling and investigations. Candidates should be thorough and detail-oriented, adhering to high quality standards in a manufacturing environment. This position provides a chance to contribute to quality assurance in healthcare technology.

Responsibilities

  • Perform inspections of purchased components and reprocessed devices.
  • Document the results of inspections and testing accurately.
  • Participate in creating and revising inspection procedures.
  • Ensure appropriate labeling and handling of products.
  • Maintain orderly quarantine areas and fulfill scrapping requests.
  • Update material status in ERP system post-activities.
  • Conduct line clearance and material reconciliation activities.
  • Assist with investigations of nonconforming products and complaints.

Job description

Performs sampling, inspection, testing, and sampling of incoming materials; conducts required in-process and final inspection of reprocessed devices their packaging; performs pre- and post-sterilization inspection of batches and review of Batch Production Records (BHRs). Strictly follows and enforces established procedures and policies needed to meet the demands of Quality in a regulated medical device company.

Essential Duties and Responsibilities:
  • Perform inspections of purchased components, reprocessed devices and their packaging, sterilization records, and Batch History Records (BHRs) to controlled procedures and pre-determined acceptance criteria.
  • Accurately document the results of the inspections and testing.
  • Participate in the creation and/or revision of procedures for the inspection function.
  • Ensures appropriate labeling, storage and handling of product and materials throughout the manufacturing facility to prevent mix-ups.
  • Ensures Quarantine areas are orderly maintained and scrapping requests made by the Materials Review Board (MRB) are fulfilled.
  • Responsible for updating material status in ERP system following the completion of Quality activities.
  • Ensures line clearance and material reconciliation activities are conducted as dictated by company procedures.
  • Assist with nonconforming product investigations, CAPAs, and customer complaints.
  • All other reasonable duties, as assigned.
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