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Outset Medical

Dialysis care technology with EMR integration

Quality Complaint Analyst

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTijuana, Baja California, MexicoNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Biomedical Engineering, Industrial Engineering, Biotechnology, or a related field.
  • At least 2 years of relevant experience in the medical device industry; experience in Quality Assurance, Complaint Handling, or Post-Market Surveillance is preferred.
  • Working knowledge of the FDA Quality Management System Regulation (QMSR), ISO 13485, and applicable U.S. medical device regulatory requirements.
  • Familiarity with FDA Medical Device Reporting requirements (21 CFR Part 803) and medical device complaint handling processes.
  • Understanding of Good Manufacturing Practices (GMP), quality management systems, and documentation practices.
  • Familiarity with complaint investigations, root cause analysis, and Corrective and Preventive Actions (CAPA).
  • Strong analytical, problem-solving, and attention-to-detail skills.
  • Ability to manage multiple priorities and work effectively in a fast-paced, cross-functional environment.
  • Proficiency in Microsoft Office; experience with electronic Quality Management Systems (eQMS) is a plus.
  • Fluency in written and spoken English.

Responsibilities

  • Contribute to continuous improvements in the Complaint Handling process.
  • Provide information for timely Adverse Event reporting.
  • Facilitate complaints throughout their lifecycle, ensuring proper documentation and timely closure.
  • Collaborate with Customer Support, Engineering, and Service teams to support complaint activities.
  • Perform reportability determinations with a medical advisor as necessary.
  • Participate in the Complaint Handling Unit and cross-functional team through completion of investigations and closure of reportable and non-reportable product complaints in accordance with company procedures and worldwide regulations and standards.
  • Comply with U.S. Food and Drug Administration regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.
  • Maintain positive and cooperative communications and collaboration with employees, customers, contractors, and vendors.
  • Maintain awareness of new or revised regulations and guidelines.
  • Develop and maintain relationships with internal and external stakeholders to support optimal performance.
  • Support additional Quality Systems activities as requested.
  • Support additional assigned activities.

Desired Qualifications

  • Excellent interpersonal skills.
  • Ability to work independently, stay motivated, and positively motivate others.

About the Company

Outset Medical

Dialysis care technology with EMR integration

Outset Medical provides an integrated dialysis program that combines the Tablo system with education and hands-on training for dialysis professionals. The Tablo device connects with electronic medical records to streamline dialysis workflows, including charting and billing, with real-time treatment updates and alerts. It differentiates itself by pairing medical hardware with staffing and transition services, offering vascular access training and Bridge programs to help facilities move from outsourcing to in-house dialysis, across hospital, clinic, and home care settings. The goal is to help hospitals and health systems deliver reliable dialysis care more efficiently by providing technology, training, and staffing support in one package.

Company size
501-1,000
Company stage
IPO
Headquarters
San Jose, CA
Founded
2010

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