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- Tasks: Design innovative medical devices and lead exciting R&D projects.
- Company: Dynamic company focused on improving healthcare through cutting-edge technology.
- Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Collaborative environment with mentorship opportunities and career advancement.
- Why this job: Make a real difference in healthcare while developing your engineering skills.
- Qualifications: 2+ years in medical devices, CAD expertise, and project management experience.
The predicted salary is between 36000 - 60000 £ per year.
ROLE PURPOSE Reporting to the Head of Research & Development (R&D), the Design Engineer presents ideas and solutions by applying a highly advanced level of specialist, detailed technical expertise to problem solving across both sides of the business (Pressure ulcer prevention & Falls Management). They are responsible for the design and development of innovative, market leading concepts and lead on assigned projects. They will plan and lead allocated projects within the R&D team, contributing to on time and budget delivery, adapting to changing circumstances promptly. The Design Engineer creates and maintains a Design History File (DHF) and other regulatory driven documentation requirements and delivers project credibility through structured development via prototyping, testing, verification, and validation. KEY TASKS & ACCOUNTABILITIES * Produce new ideas, approaches, or insights to create innovative designs through prototyping, testing & product development. * Utilise CAD to produce models, assemblies, engineering drawings (including dimensioning & tolerancing) and FEA. * Controlled implementation of documented changes in aims to improve product quality & manufacturing efficiencies. * Project management and lead on allocated R&D projects including project planning, scheduling, budgeting, and management of the project team to fulfil project goals. * Where applicable, comply with [current version] Research, Development & Design Control procedure and maintain required project documentation detailing analysis of processes and testing. * Leads on device technical files conducting remediation work where required to ensure MRD CE Marking compliance. * Support notified body technical questions as a result of audits or technical file submissions. * Identify need and select standard product testing as required. * Develop & implement product & process testing, verification, and validation protocols. * Identify & implement testing, verification, and validation of designs. * Analysis of testing, verification, and validation data. * Testing, verification, and validation report writing. * Conduct design risk management to a high level and understanding. * Signature and approver of all above reports. * Complies with policies, legal and regulatory obligations. Ensures that the design control process is adhered to according to EN ISO 13485: [current version]. * Able to suggest improvements to working practices and procedures primarily within the department but within the company too. * Where applicable, provide mentorship and professional guidance for more junior colleagues. * Prepare & manage project meetings both internally & externally e.g., suppliers, key opinion leaders etc. Skills, Qualifications and Experience * Experience: At least 2 years within the medical devices industry. * Experienced in CAD modelling & assemblies with the ability to undertake FEA and produce high quality manufacturable engineering drawings & robust designs. * Experience of working within a EN ISO 13485: [current version] Quality Management System. * Experienced in creation of technical files to support product families/groups. * Experienced in deign testing, verification and validation. * Experienced in design risk management to 14971 [current version]. * Experienced in usability engineering studies. Knowledge: Strong understanding of EU MDR, as well as international standards & regulations (ISO 13485:2016 & FDA 21 CFR Part 820 etc.) would be very advantageous. Travel: UK drivers’ licence & willingness to travel between company and customer sites as and when required
R&D Design engineer (Medical Devices) employer: Arthur Wood Recruitment
Contact Detail:
Arthur Wood Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land R&D Design engineer (Medical Devices)
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical devices field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that R&D Design Engineer role.
✨Tip Number 2
Show off your skills! Bring a portfolio of your CAD designs and prototypes to interviews. We want to see your creativity and technical expertise in action, so make sure you highlight your best work.
✨Tip Number 3
Prepare for technical questions! Brush up on your knowledge of EN ISO 13485 and design risk management. We know these topics can be tricky, but being well-prepared will show your commitment and expertise.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace R&D Design engineer (Medical Devices)
Some tips for your application 🫡
Show Off Your Skills: Make sure to highlight your experience in CAD modelling and design testing. We want to see how your skills align with our needs, so don’t hold back on showcasing your technical expertise!
Tailor Your Application: Take a moment to customise your application for the R&D Design Engineer role. Use keywords from the job description to demonstrate that you understand what we’re looking for and how you fit into our team.
Be Clear and Concise: When writing your application, keep it straightforward. We appreciate clarity, so make sure your points are easy to read and get straight to the heart of your experience and achievements.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Arthur Wood Recruitment
✨Know Your Stuff
Make sure you brush up on your technical knowledge related to medical devices, especially around CAD modelling and design verification. Be ready to discuss specific projects you've worked on and how you applied your skills in real-world scenarios.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've tackled challenges in previous roles, particularly in R&D. Think about times when you had to adapt quickly to changes or lead a project under tight deadlines, and be ready to share those stories.
✨Understand Regulatory Standards
Familiarise yourself with EN ISO 13485 and other relevant regulations. Being able to discuss how you've ensured compliance in past projects will show that you understand the importance of quality management in the medical device industry.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's current projects and future goals. This not only shows your interest but also gives you a chance to demonstrate your understanding of the industry and how you can contribute to their success.