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Telecommute Medical Data Annotation Jobs in Riverside, CA

Data Analysis: Analyze process data and quality metrics to identify trends and areas for ... Light office work and telecommuting capability. * Available to travel 20% of the time, as required ...

New

Quality Engineer I

Irvine, CA · On-site

$68K - $84K/yr

Responsibilities The Quality Engineer I will be responsible for ensuring that our medical devices ... Data Analysis: Analyze process data and quality metrics to identify trends and areas for ...

Quality Engineer I

Irvine, CA · On-site

$68K - $84K/yr

Responsibilities The Quality Engineer I will be responsible for ensuring that our medical devices ... Data Analysis: Analyze process data and quality metrics to identify trends and areas for ...

Senior Quality Engineer

Irvine, CA · On-site

$140K - $149K/yr

Compile data and prepare reports on findings, to identify trends and propose corrective action as ... May telecommute 2 days per week. Requirements: Employer will accept a Master's degree in Biomedical ...

Senior Quality Engineer

Irvine, CA · On-site +1

$140K - $149K/yr

Compile data and prepare reports on findings, to identify trends and propose corrective action as ... May telecommute 2 days per week. Requirements: Employer will accept a Master's degree in Biomedical ...

Telecommute Medical Data Annotation information

What are the key skills and qualifications needed to thrive as a Telecommute Medical Data Annotation Specialist, and why are they important?

To thrive as a Telecommute Medical Data Annotation Specialist, you need a solid understanding of medical terminology, attention to detail, and experience in data labeling or healthcare-related fields. Familiarity with annotation platforms, EHR systems, and relevant compliance certifications like HIPAA are typically required. Strong organizational skills, self-motivation, and effective remote communication set individuals apart in this remote role. These competencies ensure precise, confidential, and efficient annotation of medical data, which is crucial for supporting AI development and maintaining data integrity.

What are some common challenges faced when working remotely as a medical data annotation specialist?

As a telecommute medical data annotation specialist, one common challenge is maintaining accuracy and consistency while labeling complex medical data, especially when interpreting clinical terminology or ambiguous imaging. Working remotely can also make it harder to quickly clarify doubts or seek feedback from colleagues or supervisors, so strong communication skills and proactive outreach are important. Additionally, staying updated with evolving annotation guidelines and managing distractions at home are key factors in ensuring high-quality work.

What is telecommute medical data annotation?

Telecommute medical data annotation is the process of labeling and categorizing medical data—such as images, text, or audio—from a remote location, typically from home. This work helps train artificial intelligence and machine learning models used in healthcare, such as diagnostic tools or automated medical record systems. Annotators might identify features in radiology images, tag medical terms in documents, or classify audio recordings of doctor-patient interactions. The job requires strong attention to detail and a good understanding of medical terminology. Working remotely, annotators use specialized software provided by employers to complete their tasks securely.
What job categories do people searching Telecommute Medical Data Annotation jobs in Riverside, CA look for? The top searched job categories for Telecommute Medical Data Annotation jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Telecommute Medical Data Annotation jobs? Cities near Riverside, CA with the most Telecommute Medical Data Annotation job openings:
Quality Engineer I - Medical Device

Quality Engineer I - Medical Device

Cordis

Irvine, CA

$68K - $84K/yr

Full-time

Posted 2 days ago

New


Job description

Overview

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.

Responsibilities

The Quality Engineer I will be responsible for ensuring that our medical devices meet the highest quality standards throughout the process.  The QE I will be responsible for supporting the team through production scale up and associated quality deliverables. The primary focus will be ensuring that our processes and products meet established quality standards through developing, implementing, and continuously improving quality management systems, ensuring compliance with regulations, standards, and customer requirements. The position will collaborate with cross-functional teams to help identify quality issues, drive process improvements, and champion a culture of quality excellence.

  • Quality Control: Monitor and implement quality control measures (including verification of materials, components, and finished products) at every stage of the process, ensuring compliance with regulatory standards and internal quality requirements.
  • Process Improvement: Continuously identify and implement process improvements to enhance product quality, reduce waste, and optimize efficiency.
  • Design control: Work closely with R&D engineers to ensure design control is followed.
  • Risk Assessment: Prepare risk assessment documentation related to processes and identify potential areas for risk mitigation to ensure the safety and efficacy of medical devices.
  • Regulatory Compliance: Stay up to date with regulatory requirements, standards, and guidelines relevant to the medical device industry and ensure that processes adhere to these regulations.
  • Root Cause Analysis: Participate in root cause analysis for quality issues and recommend / implement corrective actions.
  • Documentation: Assist in maintaining accurate and complete documentation of quality-related processes, inspections, and testing, ensuring compliance with company standards.
  • Data Analysis: Analyze process data and quality metrics to identify trends and areas for improvement.
 Strategic Impact
  • Quality support to sustaining current process.
  • Quality leads to support and implementation of revised QS
 Key Interactions
  • Report on Quality Engineering.
  • Potential to interact with all functions including suppliers and customers depending on the topic/project being led or supported.
Qualifications

Required Skills and Experience

  • Bachelor's degree in mechanical engineering, Biomedical or Industrial Engineering, or other related engineering fields.
  • 2+ years in medical device production or previous internship or co-op experience in quality assurance or is a plus.
  • Previous experience working in a clean room environment [preferred]
  • Strong engineering background
  • Strong analytical and problem-solving skills.
  • Strong communication skills.
  • Excellent attention to detail and organizational skills.
  • Ability to work collaboratively in a team environment.
  • Fluent in English
Physical Requirements
  • Light office work and telecommuting capability.
  • Available to travel 20% of the time, as required domestic and international.
  • Must be able to lift and carry up to 50 lbs.

 

 

Pay / CompensationThe expected pre-tax pay rate for this position is $68,200 - $84,700. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.

Preferred Qualifications

Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammates' points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.

Employment Type: FULL_TIME