Associate Specialist, Quality Compliance

Detalles de la oferta

Associate Specialist, Quality Compliance
Apply locations Spain-Valencia

Time type: Full time

Posted on: Posted 2 Days Ago

Job requisition id: Req-37170

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Associate Specialist, Quality Compliance position is a unique career opportunity that could be your next step towards an exciting future.

Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You'll bring your passion for problem solving and partner with various teams to influence decision-making for a product's entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

Fulfill applicable medical device regulations in the region, ISO13485 and other relevant requirements for designated complaint handling unit, and evaluation of events for reportability to applicable regulatory bodies.

How You'll Make an Impact:

Investigate complaints with the support of higher level team member or manager

Evaluate event to determine if it qualifies as a complaint

Manage customer relationship and expectations during course of complaint investigation and resolution process

Assess complaint information provided and conduct additional investigation as needed and escalate as appropriate

Evaluate complaints for Medical Device Reporting to competent authorities

Prepare and submit reports to Competent Authorities, after review by more senior team member

Summarize findings, including a review of the investigation, product analysis, imaging review, instructions for use (IFU), and any other relevant labeling and/or training materials, and formulate conclusions

Prepare and submit final customer correspondence, after review by more senior team member

Other incidental duties; May identify problems with processes, procedures, and/or practices, and recommend solutions, including devising new approaches to problems encountered

What You'll Need (Required):

Bachelor's Degree in related field, 1 year experience complaint handling-similar experience Required

Experience working in a medical device (cardiovascular, endovascular, or other critical care/surgical products), healthcare, or a related environment Preferred

What Else We Look For (Preferred):

Good computer skills in MS Office Suite and ability to operate general office machinery

Good written and verbal communication skills and interpersonal relationship skills

Good problem-solving and critical thinking skills

Moderate knowledge and understanding of Edwards policies, procedures, and guidelines relevant to quality compliance

Basic knowledge of medical terms and human anatomy

Full knowledge of Medical Device Vigilance regulations, and regulatory reporting regulations

Good knowledge of Good Documentation Practices (GDP) as it relates to complaint filing

Ability to manage confidential information with discretion

Attention to detail

Ability to interact professionally with all organizational levels

Ability to manage competing priorities in a fast paced environment with guidance

Must be able to work in a team environment, including immediate supervisor and other team members in the section or group

Ability to build stable internal/external working relationships

Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

What is it like to work at Edwards Lifesciences in Spain?
As a global leader in patient-focused medical innovations, we offer rewarding opportunities and exciting challenges in a truly international, dynamic and friendly work environment.

We are committed to fostering a diverse and inclusive work environment where all employees can grow, personally and professionally. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).

Edwards Lifesciences in Spain also offers the following benefits:

Competitive Compensation and Benefits package

Flexible working hours, remote working

Pension plan

Life Insurance

Medical plan

Meal Vouchers

Service Awards

Enhanced Leave benefits

Employee Stock Purchase Programme

Employee Assistance Programme

Comprehensive Wellness programme including gym membership reimbursement, fresh fruit in the office, yoga lessons, subsidized massages, mindfulness sessions, educational events, charity activities and much more.

Benefits are regulated by an internal policy which contains the full details regarding the entitlement and conditions for the benefits. Benefits policy and components may vary by location.

About Us
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide.

For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

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