Quality Control Supervisor at CareersUSA

Fort Lauderdale, FL 33324

About the Job

CareersUSA, a leader in the staffing industry with over 36 years of experience, has another job opportunity for you:

Our Client is seeking a Quality Control Supervisor in Fort Lauderdale, FL.

Earn $36,000 per year at this full-time, permanent position.  Work 40 hours per week, Monday through Friday from 6:00 AM to 4:00 PM.

Position Summary:

Provides technical support to supplier quality program.  Applies statistical techniques to ensure appropriate sampling plans.  Develops / specifies tools to reduce inspection time and improve effectiveness of inspections. Works with other departments on the development and execution of component qualifications.  Monitors the need for supplier corrective actions and participates in supplier audits.  Must have the ability to support complaint investigations and failure analysis.   

Job Description:
  • Supervise certain quality assurance employees depending on area of supervision
  • Must be able to assess Quality System records for trends and recommend appropriate changes to sampling plans, inspections methods or tooling Recommend modifications / improvement where advisable to minimize cost and labor
  • Prepare and implement quality standards, operating procedures, inspection and test procedures and reporting systems
  • Coordinate and participate in audits whether internal or vendors to ensure a quality compliance
  • Must be able to evaluate and implement changes for efficiency and effectiveness of inspections
  • Analyzes and investigates both in house and field data, reports quality problems, recommends corrective action and follows up on the implementation and effectiveness of solutions
  • Assure all responsibilities are carried out in compliance with quality systems (i.e.ISO13485, 21CFR820) as well as all federal, state and local government regulations
  • Assist engineers in development of robust processes by using DOE and process capability techniques
  • Interface with Research and Development and other engineering departments to determine if process of product changes are needed based on investigations
  • Coordinate corrective action preventive actions internally to ensure that all failures are properly corrected and prevented from re-occurrence
  • Analyzes and prepares information on customer complaint investigations. Provides follow-up actions as necessary
  • Updates Quality Assurance procedures as necessary to comply with Quality System requirements (i.e. ISO13485, 21CFR820)
  • Assist in other areas of the Quality System not specified herein as requested
  • Conducts training programs
  • BS in Engineering or related field
  • 3 plus years of Medical Device Manufacturing or Quality experience
  • Design software (AutoCAD, Solid Works)
  • Excellent written and verbal communication
  • Understanding of quality system regulations (ISO13485, 21CFR820)
  • Ability to interact with all levels within organization
  • Analytical skills for compiling and analyzing data
  • Mechanically inclined 
  • Knowledge of DOE, SPC, Gage R&R and sampling plans
  • Computer and software skills 
  • Ability to motivate others and improve efficiency

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