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Design Quality Engineer

Galway, Ireland

R&D

Shape the Face of Cancer Treatment at Luminate Medical

Luminate Medical is on a mission to change the way we experience cancer care. We design and build products which revolutionise the patient experience of cancer treatment by eliminating that eliminate the side effects of cancer treatment in a comfortable, portable, and effective way. We’re currently building our flagship product Lily, a wearable electromechanical medical device to prevent the hair loss caused by chemotherapy, and Lilac, our next-in-portfolio electromechanical product to prevent peripheral nerve damage in chemotherapy patients.

We are looking for a Design Quality Engineer. The level of seniority can be tailored to the expertise of the suitable candidate. Working closely with R&D, Clinical, Regulatory, and Manufacturing Engineering colleagues you will provide quality expertise for our devices. You will also contribute to design for manufacturing and design for assembly considerations. Above all, you will need to enjoy working in a fast-paced environment, be passionate about working with people, and thrive in taking responsibility for delivering projects on-time to make a real world patient impact.

Working at Luminate Medical:

·This is a key early hire at a rapidly growing company. You will have an opportunity to shape the development of multiple high-impact patient-facing products and gain first-hand insights into the growth of a start-up.

·We offer a highly competitive salary comparable with (or exceeding) multinational medical device companies, a flexible benefits package, alongside a company laptop, headphones, and camera.

·Training and personal development is a key part of our culture. Comprehensive training will be provided. In addition, we will provide opportunities to develop and grow as an individual.

·We believe in quality of life in our products and for our people, and offer flexible working hours, along with a progressive personal time policy.

What You Will Do:

·Support Design Verification and Design Validation testing and associated methods.

·Lead or support corrective and preventive actions to continuously improve our designs and test methods.

·Lead or support Design Controls process and Design Reviews process.

·Support compiling technical documentation in relation to regulatory submissions.

·Support the development of test methods and associated work instructions as required

·Support Human Factors and Usability studies.

·Ensure smooth transition of activities from design to manufacturing e.g. transition of dFMEA to pFMEA, transition of Design Specifications to Manufacturing Specifications, transition of Design Test Methods to Process Test Methods, etc.

·Work with existing and future external design\manufacturing partners and suppliers.

 

Personal Attributes – The Ideal Candidate Is:

· Creative: A creative problem solver who is enthusiastic about new ideas.

· Open: You are willing to adopt, engage with and shape company culture in a positive manner. You can give and receive candid feedback in a constructive and positive manner.

· Communicative: Strong written and verbal communication and collaboration skills. You are able to articulate ideas clearly and support ideas with evidence.

· Self-Driven: You have a sense of urgency in your work, are resourceful and independent, and thrive when taking responsibility for tasks. You engage in ongoing personal development.

· Organised: You can prioritise your list of tasks independently and ensure actions are completed on time.

· Teamwork: You enjoy working in a multidisciplinary team, all working towards a common goal.

 

Experience Requirements – The Ideal Candidate Must Have:

· Qualification: Engineering, scientific or technical degree (ASQ CQE accepted)

· Experience: 3 years+ engineering experience in Design Quality or R&D.

· Within an ISO 13485 QMS or equivalent environment

· Strong experience in design controls, design reviews and design change processes

· Experience with electromechanical equipment or components or assemblies

· Strong experience in use FMEA and\or design FMEA

· Strong experience in problem-solving & root cause investigations

· Technical Skills:

· Use of statistical tools

· Proficient in MS Excel & MS Word.

· Communication Skills: Comfortable and confident communicating with internal and external stakeholders.

 

Experience Advantages – It Would Be ‘Nice to Have’/Advantageous to Have:

· Experience:

· Process or test equipment validation experience

· Previous experience working in a startup or SME environment

· Optimising processes with a view to Design for Manufacturability (DFM)

· Validating test methods and test equipment or test software

· Strong background in the use of statistical methods

 

Don’t have all of these requirements?

Some people are less likely to apply for a role unless they are 100% qualified. Your experience, skills and passion will set you apart – tell us what you have learned and achieved, whether personal or work-related! With the right mindset, many of the skills above can be learned on the job. If this role excites you, don’t let the description hold you back!

Quality Engineer
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Have questions about this role? Email us at founders@luminatemed.com.

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