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Edwards Lifesciences

Develops transcatheter heart valves and devices

Quality Compliance Specialist

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeIrvine, CA, USAIn-person

About the Job

Requirements

  • A Bachelor's degree in a related field and three years of complaint-handling experience, or equivalent work experience based on Edwards criteria.
  • Experience working in a medical device, healthcare, or related environment is required.
  • Proven expertise in the Microsoft Office Suite and ability to operate general office machinery.
  • Excellent written and verbal communication skills and interpersonal relationship skills.
  • Demonstrated problem-solving, critical-thinking, and investigative skills, with the ability to build stable internal and external working relationships.
  • Full knowledge and understanding of Edwards policies, procedures, and guidelines relevant to quality compliance.
  • Good knowledge of medical terminology and human anatomy.
  • Full knowledge of Medical Device Reporting regulations and regulatory reporting regulations.
  • Good knowledge of Good Documentation Practices as they relate to complaint filing.
  • Ability to manage confidential information with discretion and attention to detail.
  • Ability to interact professionally with all organizational levels and manage competing priorities in a fast-paced environment.
  • Ability to work in a team environment, including interdepartmental teams, and represent the department on specific projects.
  • Ability to adhere to company rules and requirements, including pandemic protocols and Environmental Health and Safety rules, and take adequate control measures to prevent injuries and protect the environment and prevent pollution within their span of influence or control.

Responsibilities

  • Assess complaint information, determine whether each event qualifies as a complaint, and escalate as appropriate.
  • Manage customer relationships and expectations throughout the complaint investigation and resolution process.
  • Research and seek information and input from Product Safety, Engineering, and other departments or business units for complaint investigations, challenging input as appropriate.
  • Identify problems and lead projects to improve processes, procedures, or practices, and recommend solutions, including devising new approaches to encountered problems.
  • Evaluate complaints for Medical Device Reporting and prepare and submit reports to the FDA.
  • Summarize findings by reviewing the investigation, product analysis, imaging, instructions for use, relevant labeling, and training materials, and formulate conclusions.
  • Prepare and submit final customer correspondence.
  • Perform other duties assigned by leadership and may assist in auditing complaint files.

Desired Qualifications

  • Experience in a medical-device environment involving cardiovascular, endovascular, critical-care, or surgical products, healthcare, or a related environment, or equivalent work experience based on Edwards criteria.

About the Company

Edwards Lifesciences

Develops transcatheter heart valves and devices

Edwards Lifesciences focuses on cardiovascular medical technologies, especially transcatheter heart valves. Its products enable repairing or replacing diseased heart valves through minimally invasive procedures rather than open-heart surgery. The company builds on a long history that began with the Starr-Edwards valve and now centers on valve therapies and related diagnostics to treat heart disease. It differentiates itself by specializing in valve technologies and transcatheter approaches, backed by a track record of clinical leadership and global reach. The goal is to improve patient outcomes by providing safer, less invasive valve treatment options for people around the world.

Company size
10,001+
Company stage
IPO
Headquarters
Irvine, CA
Founded
1958

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