Technical Author in Maidstone

Technical Author in Maidstone

Maidstone Full-Time 40000 - 50000 £ / year (est.) No working from home possible
Mirada Medical

At a Glance

  • Tasks: Create clear, user-friendly documentation for medical imaging software and support clinicians effectively.
  • Company: Join Mirada, a global leader in medical imaging technology making a real difference in cancer care.
  • Benefits: Enjoy flexible working, competitive salary, 25 days holiday, and private healthcare options.
  • Other info: Collaborative environment with opportunities for professional growth and study leave.
  • Why this job: Be part of a mission-driven team that impacts patient care and accelerates cancer treatment.
  • Qualifications: 3+ years as a Technical Author with excellent writing skills and attention to detail.

The predicted salary is between 40000 - 50000 £ per year.

Mirada is a global medical imaging company with over 2000 sites using our technology worldwide. Our mission is to accelerate cancer care by equipping clinicians and healthcare professionals with the world’s best medical imaging and AI-powered automation. We blend the scale of an established business with the fast-moving pace of a start-up. With over 1.5 million patients treated each year using Mirada products, our work makes a real difference throughout oncology and cancer care.

We’re looking for a Technical Author to own user-facing and internal documentation to support Mirada’s medical imaging software systems. You will translate complex clinical and technical functionality into clear, accurate, regulatory-compliant content that helps clinicians use our software safely and effectively. You will work as part of a multi-disciplinary team on the design, development, review and maintenance of user documentation and related materials. The role also includes development of documentation used for regulatory technical files and internal process guidance documentation.

As a Technical Author, you will be part of the Product team, working closely with Software Development, QA/RA and Product Management. As part of this role, you will:

  • Work as part of project teams to understand the product and the user documentation requirements
  • Author user documentation such as manuals, quick-start guides, how-to guides, release notes and installation guides to assist customers using our products
  • Interact with a diverse range of project team members such as Analysts, Delivery Leads, Scientists, Software Engineers, etc to develop technical documentation
  • Review, update and diversify pre-existing user documentation throughout the product life cycle
  • Contribute to the development of documentation used for technical files and regulatory submissions
  • Actively remain informed of the latest regulatory requirements for medical device user documentation
  • Create, review and assist with the elaboration of internal process guidance documents
  • Produce internal and external product training material
  • Assist with authoring and editing activities across the company that require some technical knowledge, e.g., white papers
  • Manage the translation process of product user documentation
  • Collaborate with Customer Success to adapt resources according to customer feedback
  • Collaborate with Product team to aid product requirement analysis

Skills and Experience

Essential

  • Three or more years' experience as a Technical Author
  • Excellent written English with the ability to explain complex concepts simply and precisely.
  • Strong attention to detail and a methodical approach to managing multiple concurrent deliverables.
  • Strong working knowledge of one or more technical authoring platforms (for example MadCap).
  • Comfortable working with version control (Git or SVN).

Desirable

  • Experience writing for regulated industries, preferably medical devices.
  • Familiarity with medical device standards relevant to user documentation.
  • Knowledge of medical imaging concepts or workflows, such as DICOM, PACS, or oncology treatment planning.
  • Understanding of business and user requirement elicitation.
  • Experience working in agile development methodologies.

Why work for Mirada?

  • Flexible working: Our flexible working environment is designed to work around you and your family, offering improved work/life balance
  • Holiday: We offer 25 days of annual leave (not including bank holidays). Your annual leave accrual increases by 1 day per year of service after you have been with Mirada Medical for 4 years (Max 3 Additional Days). You can also buy up to 5 additional days of annual leave and spread the cost over 11 months.
  • Competitive salary and pension: We offer an enhanced pension contribution (up to 5%).
  • Study Leave: Buy up to 5 days study leave per year and spread the cost over the remainder of the year. Mirada will also match your purchased days, doubling your study leave.
  • Private healthcare: We offer private medical and dental insurance provided by BUPA (opt-in).

Technical Author in Maidstone employer: Mirada Medical

Mirada is an exceptional employer that combines the stability of a global leader in medical imaging with the dynamic environment of a start-up. Our commitment to employee well-being is reflected in our flexible working arrangements, generous holiday allowances, and opportunities for professional development, including study leave. By joining our team, you will contribute to meaningful advancements in cancer care while enjoying a supportive work culture that values collaboration and innovation.

Mirada Medical

Contact Details:

Mirada Medical Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Technical Author in Maidstone

Tip Number 1

Network like a pro! Reach out to folks in the medical imaging field, especially those at Mirada. LinkedIn is your best mate here; drop them a message and express your interest in the Technical Author role. You never know who might put in a good word for you!

Tip Number 2

Prepare for the interview by brushing up on your knowledge of medical imaging concepts and regulatory requirements. Make sure you can explain complex ideas simply, just like you would in your documentation. This will show that you’re not just a great writer but also understand the tech behind it.

Tip Number 3

Show off your portfolio! Bring examples of your previous technical writing, especially anything related to medical devices or software. Highlight how your work has helped users understand complex systems. This will give the interviewers a taste of what you can bring to the table.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in being part of the Mirada team. Let’s get you that Technical Author position!

We think you need these skills to ace Technical Author in Maidstone

Technical Authoring
Excellent Written English
Attention to Detail
Methodical Approach
Technical Authoring Platforms (e.g., MadCap)
Version Control (Git or SVN)
Regulatory Documentation

Some tips for your application 🫡

Tailor Your Application:Make sure to customise your CV and cover letter for the Technical Author role. Highlight your experience with technical documentation and any relevant medical imaging knowledge. We want to see how you can bring your unique skills to our team!

Showcase Your Writing Skills:Since this role is all about clear communication, include samples of your previous work if possible. Whether it’s user manuals or quick-start guides, we love seeing how you can simplify complex concepts into easy-to-understand content.

Be Detail-Oriented:Attention to detail is key in this role, especially when it comes to regulatory compliance. Make sure your application is free from typos and errors, as this reflects your ability to produce high-quality documentation. We appreciate a methodical approach!

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 Mirada!

How to prepare for a job interview at Mirada Medical

Know Your Stuff

Before the interview, make sure you thoroughly understand Mirada's products and their impact on cancer care. Familiarise yourself with medical imaging concepts like DICOM and PACS, as well as the regulatory requirements for user documentation in the medical field. This knowledge will help you demonstrate your expertise and show that you're genuinely interested in the role.

Showcase Your Writing Skills

Prepare samples of your previous technical writing that highlight your ability to simplify complex concepts. Bring along manuals, guides, or any documentation you've authored that showcases your attention to detail and clarity. Be ready to discuss your writing process and how you ensure compliance with regulatory standards.

Engage with the Team

During the interview, express your enthusiasm for collaborating with diverse teams, including Software Development and QA/RA. Share examples of how you've successfully worked with cross-functional teams in the past, and be prepared to discuss how you would approach gathering user documentation requirements from various stakeholders.

Ask Insightful Questions

Prepare thoughtful questions about the role and the company culture at Mirada. Inquire about the challenges they face in technical documentation and how they measure success. This not only shows your interest but also helps you gauge if the company aligns with your values and work style.