QA TECHNICIAN

VIVOS HOLDINGS•Overland, MO
•Onsite

About The Position

The QA Technician monitors and measures quality on packaging lines to help ensure proper monitoring of fill weights, torque specifications, labels, and packaging components, along with other quality functions that support production of a good-quality product. The role works across quality assurance areas and supports compliance with cGMPs, FDA guidance documents, and customer specifications. The position is based at Page in St. Louis, Missouri, and is full-time. A high school diploma or GED is required. Two years of college-level coursework is preferred, or equivalent knowledge in math, science, and computers gained through work experience or on-the-job training. At least two years of experience in a cGMP-regulated industry is preferred.

Requirements

  • High school diploma or GED.
  • Ability to work with Microsoft Word, Access, and Excel, and an ERP system.
  • Ability to handle multiple tasks.
  • Excellent oral and written communication skills.
  • Ability to communicate cGMP standards to multiple departments and train associates on cGMPs.
  • Excellent organizational skills and attention to detail.
  • Ability to operate an electric pallet jack.

Nice To Haves

  • Two years of college-level coursework, or equivalent knowledge in math, science, and computers gained through work experience or on-the-job training.
  • At least two years of experience in a cGMP-regulated industry.

Responsibilities

  • Sample and test incoming containers and closures, and release or reject them in the computer system.
  • Inspect incoming labels for conformance to customer specifications and regulatory requirements.
  • Maintain retain samples in accordance with cGMPs and ensure samples are delivered to the QC Lab and Micro Lab.
  • Perform compounding tank inspections for cleanliness.
  • Perform special customer inspections when required.
  • Verify paperwork is accurate and complete before submitting it to the Doc Center.
  • Assist with process audits across areas involved in manufacturing drug products, including Compounding, Packaging, Receiving, Distribution, and QC labs.
  • Conduct product audits to verify in-process and packaged products meet customer specifications and cGMPs.
  • Inspect products on packaging lines and identify and report non-conforming material.
  • Work with QA Management on final disposition of quarantined and non-conforming materials.
  • Operate an electric pallet jack daily.
  • Remain flexible and work in QA areas as assigned.
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