At a Glance
- Tasks: Lead the transition of wearable medical devices from prototype to scalable production.
- Company: Innovative company focused on neuromuscular rehabilitation technology.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to innovation and patient care.
- Why this job: Make a real difference in healthcare by improving lives through technology.
- Qualifications: Experience in manufacturing processes and knowledge of medical device standards.
The predicted salary is between 40000 - 50000 £ per year.
About Neubond: Our wearable neuromuscular devices help stroke patients rehabilitate from mobility impairments through patient-centred, more accessible, and continuous care based on deep neuroscience-driven technology. This core technology has been developed in the Neurorehabilitation Engineering Lab at Imperial College London, with support from stroke patients and clinicians in London and internationally.
Role Overview: We are looking for a hands-on Production Engineer to lead the transition of our wearable medical device from engineering prototype to scale-ready, regulatory-compliant manufacturing. You will play a key role in the establishment of manufacturing processes, including supplier selection, production line setup, and test and inspection workflows—ensuring a smooth transition from prototype to scalable volume production. You will also drive design for manufacture and assembly (DfM/DfA), implement robust quality control systems, and ensure compliance with medical device standards, delivering consistent, high-quality products ready for real-world deployment.
Key Responsibilities
- Manufacturing & Design Transfer: Lead DfM / DfA activities to support the transfer from R&D to low-volume production. Develop and maintain BOMs, assembly drawings, work instructions, and test procedures. Develop and maintain process validation, continuous improvement initiatives, and root cause analysis.
- Supplier & Contract Manufacturer Management: Identify, qualify, and manage suppliers and contract manufacturers (PCBA, flex circuits, electrodes, plastics, silicone, textiles). Drive cost, quality, and lead-time optimisation across the supply chain.
- Quality & Regulatory Support: Work within an ISO 13485-compliant QMS. Support documentation for Design History File (DHF). Collaborate with regulatory consultants on regulatory standards (e.g., IEC 60601, risk management (ISO 14971), and usability engineering inputs).
Production Engineer in London employer: neubond
At Neubond, we pride ourselves on being an innovative employer dedicated to improving the lives of stroke patients through cutting-edge technology. Our collaborative work culture fosters creativity and growth, providing employees with opportunities to develop their skills in a supportive environment. Located in the vibrant city of London, we offer a unique chance to contribute to meaningful projects while enjoying the benefits of working in a dynamic and forward-thinking team.
StudySmarter Expert Advice🤫
We think this is how you could land Production Engineer in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their mission and how your skills as a Production Engineer can contribute to their goals. Tailor your answers to show you're the perfect fit!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online platforms to refine your responses. Focus on articulating your experience with manufacturing processes and quality control systems.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows your genuine interest in joining our team at Neubond.
We think you need these skills to ace Production Engineer in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Production Engineer role. Highlight relevant experience in manufacturing processes, supplier management, and quality control systems. We want to see how your skills align with our mission at Neubond!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about neuromuscular devices and how your background makes you a perfect fit for our team. Let us know what excites you about the role!
Showcase Your Problem-Solving Skills:In your application, don’t forget to mention specific examples where you've tackled challenges in production or design transfer. We love seeing how you approach problems and implement solutions—it's key for the role!
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 shows you’re keen on joining our team at Neubond!
How to prepare for a job interview at neubond
✨Know Your Tech
Make sure you understand the core technology behind Neubond's wearable devices. Brush up on neuromuscular rehabilitation and how it applies to stroke patients. Being able to discuss the science and its practical applications will show your genuine interest and expertise.
✨Showcase Your Process Knowledge
Be prepared to talk about your experience with manufacturing processes, especially in transitioning prototypes to production. Highlight any specific examples where you've led DfM/DfA activities or implemented quality control systems. This will demonstrate your hands-on experience and problem-solving skills.
✨Supplier Management Insights
Familiarise yourself with supplier selection and management. Be ready to discuss how you've identified and qualified suppliers in the past, and share any strategies you've used to optimise cost and quality. This is crucial for the role, so make it a key part of your conversation.
✨Regulatory Compliance Know-How
Understand the importance of compliance in medical device manufacturing. Brush up on ISO 13485 and relevant regulatory standards like IEC 60601. Being able to speak confidently about how you've navigated these regulations in previous roles will set you apart as a candidate.
