Job Description

Biocomposites is an international medical devices company that engineers, manufactures, and markets world-leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across Europe, USA, Argentina, Canada, China, and India. Biocomposites is a world leader in the development of innovative calcium compounds and bone cements for surgical use. Its products regenerate bone and target infection risks across a variety of specialties, including musculoskeletal infection, orthopaedics, trauma, spine, foot and ankle, podiatry, and sports injuries. Biocomposites products are now used in over one million procedures per annum and sold in more than 100 countries around the world.

Job Summary

The Regulatory Affairs Specialist (Technical Writing) is primarily responsible for leading the creation and revision of clinical evaluation reports (CER) to support regulatory submissions. They also provide support with the generation of other technical documentation (e.g. FDA Q-submissions, PSURs).

Reports to

Senior Regulatory Affairs Specialist (Technical Writing)

Location & Working pattern

Keele Science Park office. Mon-Fri, 8am-4pm or 9am-5pm

Duties & Responsibilities

• Primarily responsible for completing assigned clinical evaluation reports (CER) and other technical writing projects in a timely manner to meet business needs
• Collaborate (write, review, and edit) with R&D, clinical, technical, and regulatory teams on the creation of clinical evaluation reports, pre-submissions, and other documentation intended for regulatory submissions
• Conduct systematic literature searches for product-related data, including favourable and unfavourable data
• Critically appraise and analyse clinical data from various sources (e.g. clinical investigations, post-market activities, and vigilance systems)
• Contribute to benefit-risk profile analysis for devices and show conformance to general safety and performance requirements
• Conduct thorough quality control (QC) checks of documentation to ensure accuracy and consistency prior to approval
• Contribute to discussions focused on gaps identified in available clinical data and support with any proposed strategies to address them
• Ensure all technical writing is prepared and compliant with applicable requirements (e.g. EU MDR 2017/745, FDA Q-submission guidance, ISO standards, MDCG guidance)
• Collaborate cross-functionally to ensure the accurate drafting and presentation of technical content within clinical evaluations and technical documentation
• Provide technical writing support for global submission dossiers
• Ensure conformance with applicable requirements in product development, support of claims, content labelling, and promotional materials
• Provide Regulatory Affairs support during internal and external audits
• Handle routine correspondence and enquiries with regulatory authorities and Notified Bodies as required, under the direct supervision of senior staff
• Conduct gap assessments; report, assess, and communicate applicable changes in requirements
• Draft, update, and maintain procedures relating to clinical evaluation and technical/regulatory writing
• Mentorship of junior regulatory staff members, as required
• Provide guidance, support, and training to internal team members on clinical, technical, and/or regulatory writing and applicable requirements
• Support global submissions with clinical, technical, and/or regulatory writing requests
• Acts as a delegate for technical writing activities falling under the remit of the Senior Regulatory Affairs Specialist (Technical Writing), as needed