Product Quality Clinician (Imaging)
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 2d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 3d ago
The date the source published, not the day we noticed it (2026-09-29). Last seen at its source just now.
We have tracked this listing since 29 Sep 2026 (2 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Spain, Ireland, Portugal, United Kingdom
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $109.4k–135k/yr
Middle 50% of 20 listings that do state pay — Healthcare · all levels · EMEA · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 2d ago · last seen just now
- location not stated
The listing
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.
How you will make an Impact:
- Applies professional expertise and judgment to support product quality activities and business outcomes. Provide clinical expert knowledge and clinical guidance.
- Provide medical/clinical guidance and final direction to complaint staff and engineers related to event interpretation, event investigation, proper coding, required regulatory reporting, and complaint closure.
- Author and/or review complaint conclusions/closure statements and customer communications, including complex or novel cases.
- Evaluate information from clinical specialists, sales staff, physicians, nurses, and other hospital staff/customers, as needed to independently support complaint investigation and drive complex cases towards resolution.
- Evaluate simple and complex imaging such as Echo, Fluoroscopy, CT Scan...related to cardiovascular imaging
- Provide clinical input to Product Risk Assessments and work with Product Safety to support Decision Rationale Matrices, reporting evaluations, and other clinical or patient-risk decisions.
- Develop and deliver clinically based training to complaint staff and engineers on patient anatomy, medical conditions, products, procedures, clinical event interpretation, and applicable internal policies and procedures.
- Review regulatory submissions, regulatory agency requests, or ad hoc clinical analyzes.
- Communicate clinical conclusions, complaint data, trends, and patient-risk information to internal stakeholders in Quality, Manufacturing, Product Safety, and Product Development. Participate as clinical SME in cross-functional discussions and audits, as requested.
- Perform and/or provide clinical interpretation for additional complaint-related clinical activities, which may include review of clinical records, procedural information, literature, images, videos, or other clinical data, based on expertise and business needs.
- Identify and support process improvement opportunities, clinical standardization activities, and development or revision of relevant procedures, tools, and training materials.
- Other incidental duties
What you will need (Required):
- Bachelor's Degree or Equivalent in related field , 5 years’ of previous related experience in a Medical Device Industry, Quality System, hospital/clinical environment (i.e. cardiac care, ICU, OR, or cardiovascular/endovascular interventions)
- Moderate knowledge and understanding of principles, theories, and concepts relevant to cardiovascular imaging
What else we look for (Preferred):
- Digital capabilities (Power BI, Power Automate) and AI knowledge
- Excellent facilitation, presentation, and public speaking skills
Proven successful project management skills - Proven expertise in both Microsoft Office Suite, including advanced Excel and QMS (Quality Management System)
- Excellent documentation and communication skills and interpersonal relationship skills including relationship management skills with ability to drive achievement of objectives
- Recognized as an expert in own area with specialized depth within the organization
- Expert understanding of International Quality System Regulations
Working knowledge of Medical Device regulations, and other applicable regulatory requirements. - Provides consultancy to quality compliance team
- Consult in project setting within specific sections of quality compliance area
- Represents leadership on sections of projects within a specific area interfacing with managers and quality compliance team
- 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