Medical Writer vacatures
- Oxford Global ResourcesDe BiltAdvertentie
- Experience with higher-risk or complex medical devices.
- Proven experience supporting R&D and product development activities for medical devices.
- Thermo Fisher ScientificWerk van thuis
- Extensive proven experience as a writer of peer-reviewed medical publications (comparable to 8+ years); experience working in a CRO environment preferred.
- Thermo Fisher ScientificWerk van thuis
- Extensive proven experience as a writer of peer-reviewed medical publications.
- Our highly trained staff provide medical writing services for the peri- and post-…
- IQVIAAmsterdam
- Serve as the lead writer for key summary documents, overseeing medical writing activities across multiple compounds or programs.
- Alle vacatures voor IQVIA - Amsterdam vacatures - vacatures voor Medical Writer in Amsterdam bekijken
- Zoeken op salaris: Senior Medical Writer - FSP salarissen in Amsterdam
- Zie veelgestelde vragen en antwoorden over IQVIA
- Kuros Biosciences3723 Bilthoven
- Minimum 5 years of experience supporting medical device design and development documentation, preferably high-risk medical devices, preferably Class III…
- Alle vacatures voor Kuros Biosciences - Bilthoven vacatures - vacatures voor Technical Writer in Bilthoven bekijken
- Zoeken op salaris: Technical Writer Medical Devices and Combination Products salarissen in Bilthoven
- Zie veelgestelde vragen en antwoorden over Kuros Biosciences
- O Familiarity with medical software, specifically RIS or PACS.
- The Technical Training Specialist is responsible for designing, developing, and delivering high-…
- Alle vacatures voor DeepHealth - Amsterdam vacatures - vacatures voor Training Specialist in Amsterdam bekijken
- Zoeken op salaris: Technical Training Specialist salarissen
- O Familiarity with medical software, specifically RIS or PACS.
- The Technical Training Specialist is responsible for designing, developing, and delivering high-…
- Alle vacatures voor DeepHealth - Amsterdam vacatures - vacatures voor Training Specialist in Amsterdam bekijken
- Zoeken op salaris: Technical Training Specialist salarissen
- DentsuAmsterdam
- Communication Skills: Strong writer, presenter, and communicator who builds trust with stakeholders and maintains excellent attention to detail.
- Alle vacatures voor Dentsu - Amsterdam vacatures - vacatures voor Account Manager in Amsterdam bekijken
- Zoeken op salaris: Global Account Manager salarissen in Amsterdam
- Zie veelgestelde vragen en antwoorden over Dentsu
- Bilt RewardsBilt
- Medical Insurance (for you and your loved one) - We offer a variety of different subsidized medical plans (with dental and vision), including a free HDHP with a…
- Alle vacatures voor Bilt Rewards - Bilt vacatures - vacatures voor Social Media Specialist in Bilt bekijken
- Zoeken op salaris: Senior Manager, Social Media salarissen in Bilt
- Thermo Fisher ScientificWerk van thuis
- Ensures that all writers are adequately trained.
- Assists writers in presentation and interpretation of data.
- As a Manager Medical Writing, you will manage the…
- Alle vacatures voor Thermo Fisher Scientific - Werk van thuis vacatures - vacatures voor Medical Writing Manager in Werk van thuis bekijken
- Zoeken op salaris: Manager, Medical Writing (Publications) salarissen
- Zie veelgestelde vragen en antwoorden over Thermo Fisher Scientific
Job Post Details
Technical Writer Medical Devices - job post
Vacaturegegevens
Salaris
- € 75.000 - € 76.000 per jaar
Locatie
Volledige vacaturetekst
For an innovative medical technology company operating in a highly regulated environment, we are looking for an experienced Technical Writer to support the development of next-generation medical devices.
If you have a strong background in technical documentation within medical device development and enjoy working at the intersection of science, engineering and regulatory compliance, we would be interested in hearing from you.
Job description
This role is ideal for a professional who understands the complete product development lifecycle and enjoys translating complex technical and scientific information into clear, compliant documentation. You will work closely with multidisciplinary teams across R&D, Quality, Regulatory Affairs and Clinical functions, ensuring documentation supports both product development and regulatory approval activities.
Responsibilities
- Develop, review and maintain technical documentation throughout the full product development lifecycle.
- Support design control activities from early-stage development through verification, validation and regulatory submission.
- Contribute to Design History File (DHF) documentation and ensure traceability across development phases.
- Prepare and maintain risk management documentation in line with applicable standards.
- Support the creation of technical reports, clinical and biological evaluation documents, and regulatory submission packages.
- Collaborate with engineering, scientific, quality and regulatory teams to ensure documentation accurately reflects product development activities.
- Participate in design reviews and documentation improvement initiatives.
- Support documentation requirements for global regulatory submissions.
Requirements
- Essential minimum 5 years of experience as a Technical Writer within the medical device industry.
- Proven experience supporting R&D and product development activities for medical devices.
- Strong understanding of design controls, risk management, verification and validation documentation.
- Experience supporting products through the journey from development to regulatory registration and market approval.
- Excellent written English communication skills.
- Ability to work effectively with cross-functional stakeholders.
- Highly Desirable
- Experience with higher-risk or complex medical devices.
- Knowledge of global regulatory frameworks including EU MDR and FDA requirements.
- Experience contributing to technical documentation used in regulatory submissions.
Additional Information
- Medical Devices R&D experience is mandatory.
- Dutch language skills are not required.
- Hybrid working model with up to 3 days working from home per week.
- Competitive salary of up to €75,000 annually, depending on experience.
- Opportunity to play a key role in bringing innovative healthcare technologies from concept through to regulatory approval and commercialization.