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Data quality engineer Jobs in Miami, FL
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Quality Engineer
InspireMDMiami, FL, US- Promoted
Supplier Quality Engineer
Beckman Coulter Life SciencesMiami, FL, United States- Promoted
Senior Data Engineer
CGC Group Inc.Miami, FL, US- Promoted
Senior Data Engineer
Harnhammiami, FL, United States- Promoted
Quality Engineer
Mermaid Medical GroupSarasota County, FL, United States- Promoted
Quality Engineer
CPS ProductsHialeah, FL, United States- Promoted
Quality Engineer - AI
Millennium ManagementMiami, FL, United States- Promoted
Data Integrations Engineer
AnaplanMiami, FL, United StatesQuality Assurance Engineer
Smartcop, Inc.Florida, United States- Promoted
Data Quality Lead
Beazley GroupMiami, FL, United States- Promoted
Senior Quality Engineer
CytivaMiami, FL, United StatesQuality Engineer
EntegeeMedley, Florida- Promoted
GCP Data Engineer
Innovim Technology SolutionsMiami, FL, United StatesQuality Engineer
Lockheed MartinFlorida- Promoted
Quality Assurance Engineer II
VIVEX BIOLOGICS INCMiami, FL, US- Promoted
Quality Assurance Engineer- (Senior)
Omni InclusiveMiami, FL, United States- Promoted
Quality Assurance Engineer
Ranger Technical ResourcesBroward County, FL, United States- Promoted
Aerospace Quality Engineer
Flag SolutionsOrange, FL, United StatesQuality Engineer II
Santen IncMiami, Florida, United StatesQuality Engineer Junior
ActalentMiami, Florida, USAQuality Engineer
InspireMDMiami, FL, US- Full-time
Job Description
Job Description
Position Summary : The Quality Engineer will play a key role in maintaining and improving the quality management system (QMS) for our medical device products. You will be responsible for ensuring product compliance with FDA regulations, ISO 13485 standards, and other applicable regulatory requirements. The ideal candidate will have strong experience in the medical device industry and a solid understanding of quality control processes, inspections, and testing methods.
Essential Duties and Responsibilities : To perform this job successfully, an individual must be able to perform the following satisfactorily; other duties may be assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
- Support development, implementation and maintenance of the Quality Management System (QMS)
- Support internal and external audits to assess compliance and identify opportunities for improvement
- Support product development processes with quality planning and risk management strategies
- Conduct root cause analysis and implement corrective and preventative actions (CAPA)
- Perform product inspections, validation, and verification to ensure product quality
- Assist in the development and review of product documentation, including device master record (DMR), device history records (DHR), and technical files
- Provide support for product testing and qualification activities (e.g. design verification, validation, and stability testing)
- Work with suppliers and vendor to ensure the quality for raw materials and components
- Maintain records and reports of quality metrics, trends and performance for continuous improvement initiatives
Qualifications : To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and / or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Preferred Qualifications :
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.