Overview
$Based on experience
Full Time
Skills
IT consulting
Real-time
Quality assurance
Statistics
Industrial engineering
Medical devices
Six Sigma
Agile
SAP BASIS
Evaluation
Metrics
Policies
FDA
ISO 9000
Mentorship
Good manufacturing practice
Supervision
Data
Electrical engineering
Mechanical engineering
Job Details
Stellar Consulting Solutions is a boutique business & technology consulting company headquartered in Atlanta, GA. We deliver high quality, agile, and experienced workforce for niche technology projects of any scale. We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly
to match skill supply and demand on a real-time basis.
to match skill supply and demand on a real-time basis.
Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and retain qualified talent. We have a stellar reputation for striving to achieve high ethical standards. Our use of Innovative techniques and industry best practices has made us one of the fastest growing boutique firms delivering to enterprise business.
Title:Quality Engineer
Location: All Across USA
Job Description:
- Quality Engineering is responsible for product and service quality evaluation and control. Works cross-functionally in the development and or maintenance of products or services. The Engineer is involved in resolving the equipment and process-related production issues, activities including equipment, process, materials and method validation as well as statistical analysis and metrics to analyze those systems and processes being measured.
- Demonstrates intermediate knowledge of quality engineering policies, principles and best practices
- Demonstrates intermediate knowledge of FDA/ISO requirementsApplies statistical sample size calculations to work for quality determination on projects of intermediate scope/complexity
- May act as mentor to less experienced team membersApplies intermediate understanding of regulatory requirements (cGMP, FDA, ISO, etc.) to support work with little or no supervision
- Writes test protocol, tests, collects data, and writes reports to validate against plan to ensure product is used as intendedHas in-depth experience, knowledge and skills in own job family
- Applies knowledge and skills to a wide range of standard and non-standard situations
- Works independently with minimal guidance
- Usually determines own work priorities Acts as a resource for colleagues with less experience
Education requirements:
Bachelor's degree with 5 years of experience in a regulated environment or MS with 3 years of experience. Typical degree in Electrical or Mechanical or Industrial Engineering.
Experience:
Medical Device experience preferred
Preferred: Certification such as ASQ-CQA/CQE, AAMI, Six Sigma or a Company certification such as Green Belt, Black Belt, IGQA auditor.
Preferred: Certification such as ASQ-CQA/CQE, AAMI, Six Sigma or a Company certification such as Green Belt, Black Belt, IGQA auditor.