QA TECHNICIAN Weekend am

VIVOS HOLDINGSOverland, MO
2d

About The Position

Monitors and measures quality on packaging lines to assure proper monitoring of fill weights, torque specifications, labels and packaging components along with various quality functions to assure that production produces a good quality product.

Requirements

  • High School Diploma or GED is required.
  • Minimum of 2 years’ experience in a cGMP regulated industry is preferred.
  • Ability to work in Microsoft programs (Word, Access, and Excel) and an ERP system is required.
  • Works well with computers (ability to input or create spreadsheets, databases, etc.)
  • Demonstrated ability to handle multiple tasks.
  • Requires excellent oral & written communication skills.
  • Ability to communicate cGMP standards to multiple departments.
  • Ability to train associates on cGMPs.
  • Excellent organizational skills and attention to detail.

Nice To Haves

  • Two years of college level course work is preferred or equivalent knowledge in math, science and computers achieved from work experience and/or on-the-job training.

Responsibilities

  • Sample and test all incoming containers & closures.
  • Release or reject containers and closures in the computer system.
  • Inspect incoming labels for conformance to customer specifications and regulatory requirements.
  • Maintain retain samples in accordance with cGMPs.
  • Ensure that all samples are pulled and delivered to the QC Lab and Micro Lab.
  • Perform Compounding Tank Inspections for cleanliness.
  • Perform special customer inspections for conformance when required.
  • Assure that all paperwork is accurate and complete prior to turning into the Doc Center.
  • Assist with process audits to ensure adherence to cGMPs, FDA guidance documents and customer specifications. This includes auditing all areas directly or indirectly involved in the manufacturing of drug products; Compounding, Packaging, Receiving, Distribution, QC labs, etc.
  • Conduct product audits to ensure the in-process and packaged product meets customer specifications and cGMPs. This includes inspecting product on the Packaging lines and identifying and reporting non-conforming material.
  • Facilitate with QA Management final disposition of Quarantined and Non-Conforming Materials.
  • Must be able to operate an electric pallet jack on a daily basis.
  • Be flexible and able to work in all QA areas as assigned.
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