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Philips

Senior Validation Engineer

Posted Mar 13, 2020
Project ID: PHILJP00020755
Location
Best, Brabant
Hours/week
40 hrs/week
Timeline
8 months
Starts: Nov 1, 2019
Ends: Jul 1, 2020
Payrate range
0 - 73 €/hr
Senior Validation Engineer

Job Description:
In this role, you have the opportunity to prove that our digital pathology systems can be trusted by Pathologists in their work on cancer

Our challenge is to:
We are establishing a worldwide business for Digital & Computational Pathology. We work on the Philips Ultra Fast scanner for microscope tissue slides and an Image Management System within a Healthcare Informatics environment. Our mission is to empower pathologists with solutions so their expertise is supported by the best pathology scanners, Image Management System and workflow solutions available.

Will you help us to create solutions in a world with increasing challenges for cancer diagnostic procedures and quality of patient care?

You are responsible for:
-Managing the stakeholder input for the user and business needs, ensures the needs are compliant with good documentation principles and can be further translated into Validation protocols (Clinical, Installation & Service);
-Managing the stakeholders (end-customer, product management, system architect) during validation activities during development projects;
-Providing Validation Lead with proper validation approach information with respect to technical implementation;
-Reviewing and Validation of Claims, User and Business Needs of the products;
-Writing validation protocols based on user needs (system level);
-Supporting validation during the life cycle of a project.

You are a part of:
Philips Digital Computational Pathology (DCP) is a young and fast growing business with a global footprint. We have a deep passion and ambition to transform pathology and improve the way diagnosis is done. We have introduced products, software and services, to digitize and improve the current pathology workflow (Digital Pathology).

We collaborate in an open and informal way to drive exponential business growth at the intersection of innovation, entrepreneurship and passion - delivering cutting edge technologies that solve century old health challenges with greater speed, higher quality and better accuracy for individuals and families around the world. Join us !!!


To succeed in this role, you should have the following skills and experience:
-Master degree;
-5 years of experience in a product development environment (V-model, Agile, SCRUM);
-Experience in Pathology, Clinical Studies, Design Validation or Quality Assurance;
-knowledge of the Clinical Users, GCP (good clinical practices) & study design;
-Familiar with FDA guidance and Design Validation according to 21CFR820.30(g) and Usability engineering IEC62366;
-Self-starter, quality-conscious, excellent communicator, a problem-solver and a team player;
-Fluent in English & willing to travel.

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