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HomeCompaniesLuminatemedicalAssociate/Graduate R&D Engineer

Associate/Graduate R&D Engineer

Luminatemedical · Galway, Galway, H91 FW, Ireland · Active · BambooHR

Job facts

FieldValue
CompanyLuminatemedical
TitleAssociate/Graduate R&D Engineer
Normalized title-
Department / teamR&D
LocationGalway, Galway
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-02-16 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-04

Related slices

PageWhat it containsOpen
Company jobsActive postings from Luminatemedical.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Galway.Open
Department jobsActive postings in R&D.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyLuminatemedical
Source7a6162d6-dfb0-4a15-b647-3e5a1b153d24
ATS providerBambooHR

Description

Shape the Face of Cancer Treatment at Luminate Medical At Luminate , our mission is to make cancer care more human. Our first two products, Lily and Lilac , are revolutionary wearable devices designed to address hair loss and peripheral neuropathy respectively – two of the most common and difficult side effects of cancer treatment. We have an exciting pipeline focused on building products that help cancer patients to live, not just survive. Lotus , our latest solution is a next-generation system designed to make at-home cancer care more accessible and efficient for both patients and clinics. We’re looking for an Associate/Graduate R&D Engineer  to be a leading contributor to our Lotus SubQ device, bringing the device from design freeze through to a clinical trial. This is an exciting opportunity to be part of a multi-award-winning team and play a decisive part in the development and production of life changing devices. 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 multinational medical device companies, a flexible benefits package, alongside a company laptop, headphones and camera. We believe in quality of life in our products and for our people, and offer flexible working hours, and a generous vacation policy. What You Will Do: Contribute to the mechanical design of patient-focused cancer care products from idea to manufacture, including: Generating new design ideas and resolving design challenges by using strong understanding of fundamental engineering and design principles. Utilising CAD tools such as CREO and SolidWorks to realise product designs. Communicating design decisions, interpreting literature and test results, and influencing design direction. Producing 2D CAD drawings detailing design components and assemblies for manufacture. Creating component and material specifications. Completion of tasks and projects through a methodological and planned approach to product development. Testing, analysis and development of design concepts for novel medical devices through: Designing and building prototypes and test fixtures to prove concept effectiveness. Creating test methods to improve test repeatability. Working with users to test product designs in the real world, documenting insights and iterating on concepts. Predicting design outcomes through mathematical calculations, digital analysis, and physical design experimentation. Keeping detailed records of design and testing development work. Carrying out testing for Design Verification and Validation. Creating technical documentation according to the company’s procedures and regulatory requirements. Take responsibility for the delivery of tasks and project goals in a timely fashion by working closely with, guiding, and building relationships with external suppliers and manufacturing partners, managing their time effectively and maintaining agreed timelines. Personal Attributes – The Ideal Candidate Is: Creative:  A creative problem solver who is enthusiastic about new ideas. Open:  A proactive team player who seeks to help develop your teammates. 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 : Proficient in written and verbal communication and collaboration skills. You are able to share ideas and support exploration of other ideas. Self-Driven:  You have a sense of urgency in your work and thrive when taking responsibility for tasks. Organised : You can prioritise your list of tasks with input from more senior colleagues and ensure actions are completed on time. Experience Requirements – The Ideal Candidate Must Have: Product Development Experience:  Worked on at least 1 product design project. We prefer medical device experience but are interested in meeting candidates with design experience around consumer products. Design Skills:  CAD modelling experience (we use CREO, but we can provide training), Prototyping:  Comfortable with rapid prototyping using FDM, SLS and SLA 3D printing. Good benchtop skills for manufacturing prototypes. Experimenting:  Clear ability to create robust tests of design concepts, predict outcomes and determine iteration requirements. Experience Advantages – It Would Be Advantageous to Have: Human factors and usability engineering skills. Experience in textiles and wearables. Knowledge of plastics forming techniques such as dip moulding, blow moulding and thermoforming. Experience working within a Quality Management System. Experience with directly creating Design History File documents such as Design Input documents, Test Method Protocols, and Design Verification Protocols, alongside experience writing formal testing protocols and test reports. Experience interacting with medical device regulatory requirements and applicable standards, in particular FDA guidance, MDR guidance, ISO 13485 and IEC 60601. 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! on hold you back!

Full job record

Job ID503762e1d76a5f603a1e4153c78d3e60d8a15a4e
Org ID7316aaac-4052-4090-8b43-0307a496034c
Source ID7a6162d6-dfb0-4a15-b647-3e5a1b153d24
Board ID7a6162d6-dfb0-4a15-b647-3e5a1b153d24
Providerbamboohr
Provider Job Key79
TitleAssociate/Graduate R&D Engineer
Normalized Title
Statusactive
Activeyes
Location TextGalway, Galway, H91 FW, Ireland
DepartmentR&D
Team
Employment Typefull_time
Workplace Type
Remote Policy
Country
RegionGalway
CityGalway
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://luminatemedical.bamboohr.com/careers/79
Apply URLhttps://luminatemedical.bamboohr.com/careers/79
First Seen At2026-05-30 05:56:04Z
Last Seen At2026-06-04 11:38:31Z
Last Checked At2026-06-04 11:38:31Z
Last Changed At2026-05-30 05:56:04Z
Inactive At
Source Posted At2026-02-16 00:00:00Z
Source Updated At
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=bamboohr/board=luminatemedical/date=2026-06-04/2026-06-04T11-38-30-070Z-90a06c3e1013c5385d11721af3efe00587acd509f743e2aefecf8e88f26b84af.json
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    "description": "<p><span style=\"font-size: 12pt\"><span style=\"font-weight: bold\">Shape the Face of Cancer Treatment at Luminate Medical</span> </span></p>\n<p><br></p>\n<p><span style=\"font-size: 12pt\">At <span style=\"font-weight: bold\">Luminate</span>, our mission is to make cancer care more human.</span></p>\n<p><span style=\"font-size: 12pt\">Our first two products, <span style=\"font-weight: bold\">Lily </span>and <span style=\"font-weight: bold\">Lilac</span>, are revolutionary wearable devices designed to address hair loss and peripheral neuropathy respectively – two of the most common and difficult side effects of cancer treatment. We have an exciting pipeline focused on building products that help cancer patients to live, not just survive.<span style=\"font-weight: bold\"> Lotus</span>, our latest solution is a next-generation system designed to make at-home cancer care more accessible and efficient for both patients and clinics.</span></p>\n<p><br></p>\n<p><span style=\"font-size: 12pt\">We’re looking for an <span style=\"font-weight: bold\">Associate/Graduate R&amp;D Engineer</span> to be a leading contributor to our Lotus SubQ device, bringing the device from design freeze through to a clinical trial. This is an exciting opportunity to be part of a multi-award-winning team and play a decisive part in the development and production of life changing devices. 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.  </span></p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Working at Luminate Medical</span> </p>\n<ul>\n<li>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. </li>\n</ul>\n<ul>\n<li>We offer a highly competitive salary comparable with multinational medical device companies, a flexible benefits package, alongside a company laptop, headphones and camera. </li>\n</ul>\n<ul>\n<li>We believe in quality of life in our products and for our people, and offer flexible working hours, and a generous vacation policy. </li>\n</ul>\n<p><br></p>\n<p><span style=\"font-weight: bold\">What You Will Do:</span> </p>\n<p>Contribute to the mechanical design of patient-focused cancer care products from idea to manufacture, including:  </p>\n<ul>\n<li>Generating new design ideas and resolving design challenges by using strong understanding of fundamental engineering and design principles.  </li>\n</ul>\n<ul>\n<li>Utilising CAD tools such as CREO and SolidWorks to realise product designs. </li>\n</ul>\n<ul>\n<li>Communicating design decisions, interpreting literature and test results, and influencing design direction. </li>\n</ul>\n<ul>\n<li>Producing 2D CAD drawings detailing design components and assemblies for manufacture. </li>\n</ul>\n<ul>\n<li>Creating component and material specifications.</li>\n<li>Completion of tasks and projects through a methodological and planned approach to product development. Testing, analysis and development of design concepts for novel medical devices through: </li>\n</ul>\n<ul>\n<li>Designing and building prototypes and test fixtures to prove concept effectiveness. </li>\n</ul>\n<ul>\n<li>Creating test methods to improve test repeatability.  </li>\n</ul>\n<ul>\n<li>Working with users to test product designs in the real world, documenting insights and iterating on concepts. </li>\n</ul>\n<ul>\n<li>Predicting design outcomes through mathematical calculations, digital analysis, and physical design experimentation.  </li>\n</ul>\n<ul>\n<li>Keeping detailed records of design and testing development work. </li>\n</ul>\n<ul>\n<li>Carrying out testing for Design Verification and Validation.</li>\n</ul>\n<ul>\n<li>Creating technical documentation according to the company’s procedures and regulatory requirements. </li>\n</ul>\n<ul>\n<li>Take responsibility for the delivery of tasks and project goals in a timely fashion by working closely with, guiding, and building relationships with external suppliers and manufacturing partners, managing their time effectively and maintaining agreed timelines. </li>\n</ul>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Personal Attributes – The Ideal Candidate Is:</span> </p>\n<ul>\n<li><span style=\"font-weight: bold\">Creative:</span> A creative problem solver who is enthusiastic about new ideas.  </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Open:</span> A proactive team player who seeks to help develop your teammates. 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.  </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Communicative</span>: Proficient in written and verbal communication and collaboration skills. You are able to share ideas and support exploration of other ideas.   </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Self-Driven:</span> You have a sense of urgency in your work and thrive when taking responsibility for tasks.  </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Organised</span>: You can prioritise your list of tasks with input from more senior colleagues and ensure actions are completed on time. </li>\n</ul>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Experience Requirements – The Ideal Candidate Must Have:</span> </p>\n<ul>\n<li><span style=\"font-weight: bold\">Product Development Experience: </span>Worked on at least 1 product design project. We prefer medical device experience but are interested in meeting candidates with design experience around consumer products.  </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Design Skills: </span>CAD modelling experience (we use CREO, but we can provide training),  </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Prototyping:</span> Comfortable with rapid prototyping using FDM, SLS and SLA 3D printing. Good benchtop skills for manufacturing prototypes. </li>\n</ul>\n<ul>\n<li><span style=\"font-weight: bold\">Experimenting: </span>Clear ability to create robust tests of design concepts, predict outcomes and determine iteration requirements. </li>\n</ul>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Experience Advantages – It Would Be Advantageous to Have:</span> </p>\n<ul>\n<li>Human factors and usability engineering skills.  </li>\n</ul>\n<ul>\n<li>Experience in textiles and wearables. </li>\n</ul>\n<ul>\n<li>Knowledge of plastics forming techniques such as dip moulding, blow moulding and thermoforming. </li>\n</ul>\n<ul>\n<li>Experience working within a Quality Management System. </li>\n</ul>\n<ul>\n<li>Experience with directly creating Design History File documents such as Design Input documents, Test Method Protocols, and Design Verification Protocols, alongside experience writing formal testing protocols and test reports. </li>\n</ul>\n<ul>\n<li>Experience interacting with medical device regulatory requirements and applicable standards, in particular FDA guidance, MDR guidance, ISO 13485 and IEC 60601. </li>\n</ul>\n<p><br><br></p>\n<p><span style=\"font-weight: bold\">Don’t have all of these requirements?</span> </p>\n<p>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!</p>\n<p> </p>\n<p><span style=\"color: rgba(0, 0, 0, 0); font-family: sans-serif; font-size: 10pt\">on hold you back!</span></p>",
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