At a Glance
- Tasks: Create and manage technical documentation for innovative medical devices.
- Company: Established healthcare manufacturer focused on improving patient outcomes.
- Benefits: Competitive salary, career growth, and a chance to make a difference.
- Other info: Dynamic work environment with a focus on continuous improvement.
- Why this job: Join a team dedicated to innovation and compliance in the medical field.
- Qualifications: Experience in technical documentation and CAD modelling is essential.
The predicted salary is between 40000 - 50000 £ per year.
A Technical Documentation Development Engineer is required to support medical device product development through robust documentation, CAD formalisation, and regulatory compliance. The role focuses on ensuring all new and legacy products meet MDR requirements, with a strong emphasis on technical file ownership, structure, and accuracy.
Client Details: This is an established healthcare manufacturer operating within a regulated medical device environment, focused on improving patient outcomes through product innovation and continuous improvement. The business has a growing portfolio of products and is investing in strengthening its documentation, compliance, and development processes.
Description
Key responsibilities:
- Produce and maintain technical documentation in line with MDR requirements
- Build, manage, and update Technical Files for both new and legacy products
- Take ownership of legacy documentation, including reverse engineering and generating CAD models/drawings
- Create production-ready, revision-controlled CAD drawings from existing products and development inputs
- Document all design changes, improvements, and development activities
- Ensure compliance with medical device regulations, standards, and internal gated processes
- Support risk management activities and maintain structured design documentation (e.g. DHF)
Technical Documentation and Development Engineer employer: Michael Page Engineering & Manufacturing
As a leading healthcare manufacturer, we pride ourselves on fostering a collaborative and innovative work environment that prioritises employee growth and development. Our commitment to improving patient outcomes is matched by our dedication to providing comprehensive training, competitive benefits, and opportunities for career advancement within the regulated medical device sector. Join us in making a meaningful impact while enjoying a supportive culture that values your contributions and encourages continuous improvement.
Contact Details:
Michael Page Engineering & Manufacturing Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Technical Documentation and Development Engineer
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at local meetups. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Showcase your skills! Create a portfolio that highlights your technical documentation and CAD work. We want to see your best projects, so make sure it’s easy to access and visually appealing.
✨Tip Number 3
Prepare for interviews by brushing up on MDR requirements and regulatory compliance. We recommend practising common interview questions related to technical documentation to boost your confidence.
✨Tip Number 4
Apply through our website! It’s the quickest way to get your application noticed. We’re always on the lookout for passionate candidates who are ready to contribute to our mission of improving patient outcomes.
We think you need these skills to ace Technical Documentation and Development Engineer
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Technical Documentation and Development Engineer role. Highlight your experience with technical documentation, CAD formalisation, and any regulatory compliance work you've done. We want to see how your skills match what we're looking for!
Showcase Your Projects:Include specific examples of projects where you've produced or maintained technical documentation. If you've worked on medical devices or similar regulated environments, let us know! This will help us understand your hands-on experience.
Be Clear and Concise:When writing your application, clarity is key. Use straightforward language and avoid jargon unless it's relevant. We appreciate a well-structured application that gets straight to the point, especially when it comes to your technical skills.
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to upload all your documents in one go. Plus, it helps us keep track of your application better!
How to prepare for a job interview at Michael Page Engineering & Manufacturing
✨Know Your MDR Inside Out
Make sure you’re well-versed in the Medical Device Regulation (MDR) requirements. Brush up on how they apply to technical documentation and be ready to discuss specific examples of how you've ensured compliance in past projects.
✨Showcase Your CAD Skills
Prepare to demonstrate your proficiency in CAD software. Bring along examples of your previous work, such as production-ready drawings or models, and be ready to explain your design process and any challenges you faced.
✨Highlight Your Documentation Experience
Be prepared to talk about your experience with technical documentation. Discuss how you’ve managed technical files, including any reverse engineering tasks, and how you ensure accuracy and structure in your documentation.
✨Emphasise Continuous Improvement
This role is all about innovation and improvement. Share examples of how you’ve contributed to product development processes in the past, focusing on how you’ve implemented changes that improved compliance or efficiency.
