Quality Control Specialist

The Job Holder
Savannah, GA, USA
Aug 24, 2019

Client Name

Brasseler USA


Brasseler USA® is an ISO-affirmed imaginative, accuracy dental and therapeutic instrumentation organization headquartered in Savannah, Georgia. The educated, profoundly prepared, agreeable Brasseler USA deals group works with dental and medicinal human services experts day by day to convey uncommonly, demonstrated, unsurprising, made-in-the-USA items that enable perceiving specialists to convey quality consideration. Brasseler USA's commitment to finding the opportune individual for the correct position guarantees that representatives are cheerful, tested and satisfied in their work. The organization offers its workers open doors for learning and development and perceives the significant commitments its colleagues make to the achievement of the association. 



Employment OVERVIEW: 


This position is in charge of helping the Manager of QA/RA in taking care of a wide scope of Quality Systems administrative prerequisites and related quality exercises in our dental and therapeutic organizations. The individual helps with examining and supporting administrative issues exercises, aids the advancement of methods, and directions with various divisions to guarantee quality framework prerequisites are met. 





  • Audit records and archives, for culmination and consistency with Quality System Requirements and ISO prerequisites. 
  • Aid all-inclusive preparing on general quality standards and explicit procedural necessities. 
  • Educate and lead others in creating quality abilities. 
  • Aid the advancement of standard working strategies to characterize and improve quality framework capacities. 
  • Start quality framework process improvement 
  • Oversee and keeps up Quality System archives and records 
  • Bolster the Corrective Action program, with hands-on proprietorship for examination and goals of issues. 
  • Help, facilitate and take an interest in quality framework reviews and administrative investigations. 
  • Bolster the Material Review Board, for the evaluation and mien of non-acclimating materials and conclusion of Non-conformance and Deviation Reports. 



Research quality issues 


  • Aid the culmination of fundamental data and submits archives required to enlist items, acquire licenses, report antagonistic occasions, and different entries as coordinated by the Manager of QA/RA. 
  • Encourage process improvement inside different divisions, using preparing, instructing, and group cooperation. 
  • Direct process quality estimations/assessments 
  • Cooperates with Product Management to help and organize required accommodation documentation 
  • Helps to observe, breaking down and detailing patterns in key quality measurements. 
  • Guarantees built-up office timetables are achieved. 
  • Different exercises as doled out by the Manager of QA/RA 





  • Applicable involvement in the therapeutic gadget industry is liked. 
  • Nature with FDA restorative gadget guidelines liked. 
  • Nature with ISO 13485, CMDR and EUMDD liked. 





  • Partners Degree and four years of related involvement. 



Information, SKILLS, and COMPETENCIES: 


  • Capacity to peruse and decipher general specialized/quality methodology and quality framework guidelines. 
  • Capacity to make reports, business correspondence, and method manuals 
  • Capacity to viably exhibit data and react to questions verbally, recorded as a hard copy, and in gathering introductions 
  • Must be gifted in Microsoft Word, Excel, Outlook and PowerPoint 





  • Travel regularly under 10%. Office condition. No uncommon physical requests required. 
  • Employment requests may require significant lots of sitting, standing, phone work, and PC work 
  • Occupation requests may require periodic hard work, as much as 15 pounds.