At a Glance
- Tasks: Lead the creation of regulatory documents for medical devices and collaborate with diverse teams.
- Company: Biocomposites, a forward-thinking company in Keele, UK.
- Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to advancing medical technology.
- Why this job: Make a difference in healthcare by ensuring compliance and safety of innovative medical devices.
- Qualifications: Experience in regulatory writing and strong technical writing skills required.
The predicted salary is between 63000 - 77000 £ per year.
Biocomposites, based in Keele, UK, is seeking an experienced Regulatory Affairs Specialist (Technical Writing) to lead CER creation and revisions to support regulatory submissions.
You will collaborate across R&D, clinical, regulatory, and technical teams to compile robust documentation for EU MDR 2017/745 and FDA Q-submission processes.
The role requires expert literature searches, critical data appraisal, and high-quality technical writing with attention to regulatory guidelines.
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Medical Device Regulatory Writing Specialist employer: Biocomposites
Biocomposites in Keele, UK, is an excellent employer that prioritises collaboration and employee growth, making it an ideal place for those looking to advance their careers in a supportive environment. With a strong focus on safety and reliability, employees benefit from comprehensive training and development opportunities, ensuring they are well-equipped to lead maintenance activities effectively. Join us to be part of a dynamic team dedicated to innovation and excellence in the biocomposite industry.
