iRhythm Technologies, Inc.

Quality Specialist - Post Market

iRhythm Technologies, Inc.$74K — $93K *
US-AnywhereRemote in United States
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or Associate Degree in science, technology, or medical fields
  • 2 years of experience in Quality Assurance or complaint processing
  • Knowledge of global medical device regulations for complaint handling
  • Proficient in vigilance and post-market surveillance reporting
  • Strong written and verbal communication skills

Responsibilities

  • Evaluate complaints for reportability under various regulatory requirements
  • Conduct and oversee moderately complex complaint investigations
  • Analyze technical data for root cause assessments
  • Collaborate with cross-functional teams for investigations
  • Identify and escalate trends or issues found during investigations
  • Support process improvements and quality initiatives
  • Perform additional related duties as assigned

Benefits

  • Remote work flexibility within the US
  • Engagement in a critical area of medical device quality assurance
  • Opportunity for professional growth in a regulatory environment
  • Collaborative cross-functional teamwork
  • Impact on product safety and customer satisfaction
Full Job Description
About This Role:

About this role:

The QA Specialist - Post Market is a developing professional who independently manages routine to moderately complex complaints and applies regulatory knowledge within defined frameworks. Duties include, but are not limited to, day to day complaint review, investigation reports, adverse event reporting and complaints log and trend maintenance.

Responsibilities:
• Independently evaluate complaints to determine reportability in accordance with USA, European and Japan adverse event reporting requirements with guidance
• Perform and/or coordinate moderately complex complaint investigations in a timely manner
• Analyze technical information to support root cause assessment using established methods
• Collaborate cross-functionally to complete investigations
• Identify trends and/or issues for escalation
• Identify opportunities for and support process improvements
• Perform other quality and regulatory-related duties as assigned

Required Qualifications:
• Bachelor's Degree or Associate Degree in science, technology or medical fields
• 2 years of experience in Quality Assurance and / or a complaint processing role
• Working knowledge of applicable global medical device regulations particularly as they relate to complaint handling, vigilance, reporting timelines, and post-market surveillance
• Strong written and verbal communication skills

Location:
Remote - US

Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.

Estimated Pay Range
$74,000.00 - $93,000.00

About iRhythm Technologies, Inc.

iRhythm Technologies is a medical device company that develops and commercializes solutions for cardiac arrhythmia detection. The company's flagship product is the Zio XT, a wearable patch that continuously monitors a patient's heart rhythm for up to 14 days. The Zio XT is designed to improve the detection and diagnosis of cardiac arrhythmias, which can be difficult to diagnose due to their intermittent nature. iRhythm Technologies was founded in 2006 and is headquartered in Redwood City, California. The company went public in 2016 and is traded on the NASDAQ stock exchange under the ticker symbol IRTC.
Learn more about iRhythm Technologies, Inc.
Size
1,700 employees
Market Cap
$2.7 billion
Industry
Net Income
-$43.8 million
Founded
2006
5 Year Trend
+38.2%
Revenue
$265.1 million
NASDAQ

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