At a Glance
- Tasks: Lead usability engineering for innovative implantable medical devices, ensuring user-friendly designs.
- Company: Join a pioneering medical technology company making a real impact in healthcare.
- Benefits: Enjoy hybrid working, competitive salary, shares, private healthcare, and more perks.
- Why this job: Shape the future of medical technology while collaborating with diverse teams and mentoring others.
- Qualifications: Strong background in human factors engineering for regulated medical devices is essential.
- Other info: Opportunity to travel across Europe and influence real-world clinical experiences.
The predicted salary is between 48000 - 72000 £ per year.
Principal Human Factors Engineer – Implantable Medical Devices – Oxford We\’re partnering with a pioneering medical technology company to recruit a Principal Human Factors Engineer who will shape how clinicians and surgical teams interact with transformative implantable devices. This is a rare opportunity to lead usability engineering across the full product lifecycle, embedding human-centred design into every stage of development and ensuring that systems are safe, effective, and intuitive to use. The role is based in Oxfordshire and offers hybrid working, with three days on-site including Tuesdays and Wednesdays. Occasional travel to third-party sites across Europe will be required, so a willingness to travel is essential. This is a direct hire with a medical devices company – not a design consultancy. In this role, you\’ll be responsible for developing and delivering the company\’s usability strategy in line with international standards and regulatory frameworks. You\’ll lead formative and summative studies in clinical and simulated environments, translating user insights into actionable design inputs and risk management decisions. You\’ll collaborate across engineering, clinical, regulatory, and quality teams to embed usability as a guiding design principle, not just a compliance checkbox. You\’ll take ownership of the usability engineering file, contribute to global submissions, and represent human factors in audits, design reviews, and stakeholder presentations. Your work will span cadaver lab studies, system integration testing, and continuous evaluation of user experience across a portfolio of implantable medical technologies. You\’ll also mentor internal teams, manage external partners, and help foster a culture of user advocacy and design excellence. To succeed in this role, you\’ll bring a strong background in human factors engineering for regulated medical devices, ideally with experience in surgical or implantable systems. You\’ll be comfortable leading usability studies, navigating international regulatory expectations, and translating complex user needs into clear design requirements. A proactive mindset, excellent communication skills, and a deep empathy for users will be key to your success. This is more than a technical leadership role – it\’s a chance to influence how innovative medical technologies are experienced in real-world clinical settings. If you\’re passionate about usability, design, and making a meaningful impact, we\’d love to hear from you. Alongside the opportunity to lead impactful work, this role offers a competitive package including shares/equity, life assurance, pension, private healthcare, income protection, and an employer discount scheme – benefits more commonly found in larger organisations. To learn more, contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your CV and a member of our team will be in touch
Principal Human Factors Engineer - Implantable Medical Devices employer: Newton Colmore
Contact Detail:
Newton Colmore Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Human Factors Engineer - Implantable Medical Devices
✨Tip Number 1
Familiarise yourself with the latest international standards and regulatory frameworks related to human factors engineering in medical devices. This knowledge will not only help you understand the expectations of the role but also demonstrate your commitment to compliance and safety during interviews.
✨Tip Number 2
Network with professionals in the medical device industry, particularly those involved in usability studies and human factors engineering. Attend relevant conferences or webinars to connect with potential colleagues and gain insights into current trends and challenges in the field.
✨Tip Number 3
Prepare to discuss specific examples from your past experience where you've successfully led usability studies or implemented user-centred design principles. Highlight how these experiences have positively impacted product development and user satisfaction.
✨Tip Number 4
Showcase your ability to collaborate across various teams by preparing examples of how you've worked with engineering, clinical, and regulatory teams in previous roles. Emphasising your teamwork skills will be crucial, as this role requires a strong collaborative approach.
We think you need these skills to ace Principal Human Factors Engineer - Implantable Medical Devices
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities and requirements of the Principal Human Factors Engineer position. Familiarise yourself with usability engineering principles, especially in the context of implantable medical devices.
Tailor Your CV: Customise your CV to highlight relevant experience in human factors engineering, particularly with regulated medical devices. Emphasise any leadership roles you've held in usability studies and your ability to navigate regulatory frameworks.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for usability and design in medical technologies. Mention specific experiences that demonstrate your skills in leading usability studies and collaborating with cross-functional teams.
Highlight Your Communication Skills: In both your CV and cover letter, emphasise your excellent communication skills. Provide examples of how you've effectively communicated complex user needs to diverse stakeholders, as this is crucial for the role.
How to prepare for a job interview at Newton Colmore
✨Understand Human Factors Engineering
Make sure you have a solid grasp of human factors engineering principles, especially as they relate to regulated medical devices. Be prepared to discuss how you've applied these principles in past projects, particularly in surgical or implantable systems.
✨Showcase Your Usability Studies Experience
Highlight your experience leading usability studies, both formative and summative. Be ready to share specific examples of how user insights influenced design decisions and improved product usability.
✨Familiarise Yourself with Regulatory Standards
Brush up on international regulatory expectations related to usability in medical devices. Demonstrating your knowledge of these standards will show that you can navigate compliance effectively while prioritising user experience.
✨Emphasise Collaboration Skills
This role requires collaboration across various teams. Prepare to discuss how you've successfully worked with engineering, clinical, regulatory, and quality teams in the past, and how you can foster a culture of user advocacy within those groups.