Job Description

Quality Engineer

Location: Daytona, FL area

About the job: Company is a global leader in manufacturing and the distribution of innovative home and long-term care medical products. Headquartered in the U.S., our client employs over 4,500+ individuals and markets their products in 80 countries around the world. We are seeking a Quality Engineer who is, in part ─ able to apply and analyze situations related to regulatory, documentation, design, risk analysis, audit, corrective action, product development, pre and post market, and supplier management requirements This is an exciting opportunity for a top performer to establish themselves with a worldwide leader with absolute opportunities for advancement!

Job Description:

  • The Quality Engineer will participate, implement, or understand new strategies, processes and policies as it relates to good manufacturing practice requirements, validation, design input, rework, audits, complaint, component and control.
  • Your role at the facility will be to evaluate and implement methods, definitions, and principles as it relates to their functional area of quality and share that knowledge and experience to the newer members of the team.
  • Translates strategy into executable plans by working collaboratively across functions with guidance.
  • The Quality Engineer will determine the appropriate standard quantitative methods such metrology, data analysis, statistical process control, etc. across a spectrum of business environments to facilitate process analysis and improvements with little direction.
  • You will participate in the quality audit process including, preparation, reporting results and follow-up.
  • Review and act on governmental changes that impact company policy, procedures and documentation.
  • Provides support on the development and exploration of new and innovative products, services and partnerships that drive growth and leverage the company’s worldwide capabilities.
  • Partakes in projects to drive continuous improvement to processes within the business/function.
  • Recognize and accurately interpret the communication of others as expressed through various mediums.
  • Collaboratively work with manager to establish self-development plans that identify learning opportunities and activities that will help achieve individual goals.
  • Complete all required training applicable to assigned position.

Job Requirements:

  • Bachelor’s degree in Engineering, Science, or Quality required. Master’s degree preferred
  • 3 years of experience in a progressive manufacturing operations or quality environment required.
  • Currently hold or working toward Certified Quality Engineer and/or Six Sigma, Black Belt, LEAN, Quality Auditing etc. certifications
  • Will have experience and understanding in two or more cross functional areas (regulatory, documentation, design, risk analysis, audit, corrective action, product development, pre and post market, and supplier management).
  • Working knowledge and practical experience of FDA’s QSR and ISO9001 or ISO13485 quality systems.
  • Ability to work independently in a fast-paced environment and to drive change.
  • Proven problem solving and analytical abilities.

Salary: $65,000 - $80,000

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