Biocomposites, based at Keele Science Park, is seeking a Regulatory Affairs Specialist (Technical Writing) to lead CER creation and other regulatory documentation for submissions. You will collaborate across R&D, clinical, regulatory and quality teams to ensure accurate, compliant reporting under EU MDR 2017/745 and related guidelines.
The role requires 5+ years in medical writing within pharma/medical devices, with strong knowledge of regulatory submissions and regulatory guidance.
#J-18808-LjbffrRegulatory Medical Writer – Device Submissions & CERs in Keele 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.
