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Idoven is hiring a
Regulatory Affairs Technical Writer

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Read by 189 job seekers.

Madrid, Spain

About us

Idoven has developed the world’s first cardiology-as-a-service platform powered by artificial intelligence that augments both a cardiologist’s and non-cardiology expert clinician’s ability to identify, triage and diagnose patients at scale.

The company counts partners such as AstraZeneca, Abbott, and GE Healthcare, FIFPRO, Google, Santander and Real Madrid Foundation. Idoven is backed by top-tier investors and business angels including Insight Partners, Northzone and Wayra (Telefónica), Iker Casillas, Pau Gasol, the Accel Starters program, and EIT Health.

The company has been awarded with numerous distinctions for its AI technology in Europe and the US, including the prestigious European Innovation Council (EIC) Accelerator and Horizon 2020 (H2020) awards and the Healthy Longevity Catalyst Award from the US National Academy of Medicine. Idoven has also been selected by CB Insights as one of the top 50 companies in Digital Health for 2023.

What you will do

Duties include collaboration with cross-functional teams including Design and Development, RA/QA, Marketing, People and other relevant functions to create and maintain technical documentation, procedures, customer facing documentation and records. The Technical Writer is also responsible for writing and/or editing procedural documentation, product documentation, reference manuals, product manuals, regulatory/quality documentation and any other documentation as required.

Responsibilities

• Create documentation across the company with high degree of quality

• Develop method to standardize the technical writing process

• Support multiple functions in the production of documentation

• Develop content for internal, external, and client-facing documentation

• Work together with relevant teams and departments to create, edit and maintain relevant documentation

• Ensure all documentation meets current APA standards of English

Requirements

• Bachelor’s degree or experience in related field (Master’s degree a plus)

• Min. 2 years experience in writing and editing technical documents

• Fluency in English is required

• Experience with Medical Device Technical Documentation for the EU MDR and the US FDA (21 CFR)

• Strong analytical and problem-solving skills

• Excellent verbal and written communication skills

• Ability to translate complex technical concepts and present them to the intended audience in a clear and understandable way

• Ability to work efficiently in a team environment and to function with a high level of autonomy

• In-depth attention to detail and accuracy with the ability to prioritize and work on multiple projects in a fast-paced, start-up environment

• Basic understanding of software development life cycle is a plus

Benefits

🚀 Be part of one of the most disruptive startups in HealthTech and AI and make a difference

🏆 Personal and professional growth as part of a fast-growing, international team

🎧No corners cut in having the best tech equipment to do your job

🙋 Flexible remote working environment, where you can choose to work from home and come to our Madrid office whenever you want to

💸 Flexible Remuneration. We give you the flexibility to consume your benefits (from meals, transportation, kindergarten, training, and health insurance) directly from your payroll and receive tax benefits (Spain only)

😎 Regular team events and Thursday happy hours


And much more!

At IDOVEN, we believe in hiring top talented people like you - ambitious, forward thinkers who want to make a difference in the world and have an impact. Apply now via the apply button or contact us via talent@idoven.ai .

Estimated Salary range:

Our salary intelligence, powered by our AI algorithms, has calculated an estimated range for this position between €40,000 - €50,000 . Please note that the actual salary for this position may vary, as it is dependent on various factors including but not limited to experience, location, and market dynamics.

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