Technical Writer

Medimaps Group is a leading global medical software analytics company designing, developing and commercializing AI powered medical imaging software for assessing bone health and improving fracture risk detection. At Medimaps, we strive to find simple solutions to complex medical needs for the benefit of the patient. Our passion is to make meaningful and efficient products based on technological innovation.

 

Headquartered in Plan-les-Ouates, Geneva, Switzerland, with offices in the US and France, we are rapidly scaling up and looking to transition into the next phase of our growth plan. To support us on on scale up journey we are actively seeking to fill the newly created role of Technical Writer

 

Reporting directly to the CPTO and collaborating with the Software Development & RAQA Teams the Technical Writer will be responsible for good document practice for all medimaps products.

 

This is a rare and exciting opportunity for a highly motivated, and ambitious candidate looking to join a fast-growing business with real potential for value creation and career development.

 

Interested? Then please keep reading.

 

Key Responsibilities:

 

  • Writing technical documentation to the high-quality level and standards required
  • Controlling and improving the level of quality of existing documentation
  • Interacting with the team to ensure consistency and alignment of documentation with the relevant medical device software, applications and their associated devices or products
  • To following Good Documentation Practice
  • Ensure the complete list of documentation required, according to the process
  • Prepare instruction manuals
  • Prepare medical user guides and training materials for healthcare professionals
  • Prepare a broad range of marketing collateral by collaborating with the product managers
  • Create medical device user manuals
  • Disseminate technical information in easy-to-understand, concise language for a non-technical audience
  • Have technical accuracy in writing user documentation
  • Collaborate with subject matter experts and technical staff to create accurate and detailed software documentation
  • Assist other writers in creating documentation
  • Create product manuals with screenshots and tutorials
  • Write documentation for internal teams such as developers and programmers

 

 

What You'll Need To Succeed

  • Bachelor’s degree , MS degree in Quality, or Biomedical Engineering or related field; or Information Systems, Information Technology, Computer Science, or other related disciplines applied to Software as Medical Device Development
  • 3 to 5 years of good documentation practice in medical sectors
  • Knowledge in methodology and practices in software development
  • Ability to understand and explain technical complex relative to AI, SaaS, Software
  • Very strong skills in Microsoft Office (Word, Excel)
  • Strong experience in writing technical documents (GDP): Requirements, Needs, SOP, Specifications, protocols, etc.
  • Good experience in writing & reviewing documentation for medical device development
  • Experience with Application Requirements Management software or Document Management software, ALM such as Jama-connect, Polarion, IBM, Jira, Agile, Google Docs, etc.
  • Strong analytical skills & details oriented
  • Ability to undertake multiple projects and deliver on tight deadlines
  • Excellent technical writing skills in English and French
  • Excellent verbal communication skills
  • “Getting things done”, being hands-on and thinking strategically is natural for you
  • You enjoy thinking outside of your area of work and to actively drive business decisions
  • You are a team player, humble, lead by example and have a good sense of humour
  • Confident and proactive, with the ability to take the lead in challenging situations
  • Swiss / EU citizen or current holder of Swiss work permit. Currently living or are willing to move to /close to Geneva, Switzerland
  • Fluent English speaker (with professional level French a plus)

 

What You Will Receive In Return

  • The security of working in an innovative developing company with a sustainable business model
  • The opportunity to work on interesting and challenging cross functional projects across teams
  • Working with an international, multi-cultural and socially responsible company with meaningful corporate values and an inspiring mission
  • Working with a genuinely great bunch of talented, professional and friendly people, who work hard but know how to have fun and make work a real pleasure
  • An attractive compensation package

 

If this job inspires you and you would like to join the medimaps team, please apply immediately via our LinkedIn Recruitment Platform.

 

Candidates whose profiles do not meet our needs at this time will be notified at the end of the recruitment process. We anticipate that this may take approximately two months. We apologize in advance for this potential delay but will do our best to get back to you at the earliest possible opportunity.

 

We are looking forward to receiving your application and to getting to know you better!