Requirement and Test Engineer

le contenu du travail

The company

In 2020, we decided to launch P³Lab with a team of doctors and engineers to help our healthcare system jump the chiasm of technology. We believe in cross fertilization allowing to find answers to complex healthcare problems amongst other existing fields. We are committed to positively impact humankind and give a small fraction back of what our society has invested in us. We want to provide Pragmatic healthcare innovation to emPower People.

Our first mission is to develop and propagate an eye-tracking lab to help objectively diagnose neurologic diseases and treat vision disorders through instant quantification of the clinical examination.

We are now fully funded and are looking for a collaborator in this adventure as we strongly believe in the capacity of collective intelligence to tackle intricate issues.

Will you be the one we are looking for?

Job Description

The team is currently looking for a highly motivated Developer.

You will work alongside with a team of developers and engineers in close collaboration with our CTO, our Product manager and our Head of QARA.

Your primary focus will be defining the supporting back-end , implementing, testing and verify it.

You will ensure that our solution (NeuroClues) is safe, effective, and compliant with medical device standards.

Candidate

General Mission

As a Requirements and Test engineer in the Innovation and Development team, you will take part in the design and development of a new medical device intended for recording, viewing, and analyzing eye movements.

Main responsibilities

You will share responsibility of the management of system requirements and system verification for an effective product with the highest customer value. In this role, you will ensure that your work complies with the highly regulated environment of medical applications :

• You ensure requirements engineering activities for the new product and well as future product changes. You negotiate with project stakeholders, allocate and flowdown system requirements, trace them and document them in a complete and consistent way;
• You participate in safety and reliability engineering activities throughout the design and development phase;
• You ensure design verification engineering by defining test plans, test methods, analyses, design reviews and performing tests (SW and HW);
• You take part in the improvements of system engineering methods and tools by collecting, suggesting and implementing changes in agreement with the experts.

Required competencies

You have (required):

• A degree in Science or (Biomedical) Engineering; with a multidisciplinary background or in the following disciplines: SW engineering, electrical engineering, biomedical engineering;
• Excellent oral and written communication skills in English.

You have one or more of the following experiences (preferable):

• Applied requirements engineering and verification techniques;
• Application of regulatory and quality constrains in a critical and complex environment. Medical devices framework is a plus.
• Interaction with internal and external third parties, including Product Management representative, customer representative, third-party representatives, regulatory authorities;
• Use and maintenance of a Requirements and test management tool (Jira & XRay)

And you are:

• A team player able to communicate / facilitate / focus on promoting solutions;
• Capable of thinking cross-functionally and systems thinking;
• Structured and rigorous on the documentation part;
• Quality focused, working for the highest value for your stakeholders

What do we offer

• An Empowering organization with a strong culture of Trust, Respect, Quality, and Pragmatism
• 80%, 90% or 100% Permanent Contract
• Work from anywhere in Belgium policy
• Attractive salary package
• A fun to work with team
• A great possibility to have a positive impact on patients

Apply if you are interested.