We are looking to recruit a Technical Documentation Specialist who will be responsible for compiling and maintaining documentation for our medical devices, ensuring compliance with the Medical Device Regulation (EU) 2017/745 and the UK Medical Devices Regulations (UK MDR 2002, as amended). This position will be joining our thriving UK medical device manufacturing company to work within our Design and Development Department. The successful candidate will be able to work closely with multiple departments to support updates and submissions for product audits, manage documentation and maintain traceable records to support regulatory compliance and audit readiness, and contribute to the clarity and consistency of our records across the organisation.

This role requires adaptability, focus, and the ability to manage shifting priorities in a fast-paced environment. It is ideal for someone who thrives on detail, enjoys cross-functional collaboration, and is eager to grow within the medical device industry.,

• Excellent organisational skills and attention to detail
• Clear and confident written and verbal communication
• Strong administrative and IT skills, including MS Office (especially Word and Excel)
• Ability to follow procedures and work instructions precisely
• Ability to work independently and as part of a team in a dynamic environment
• Self-motivated with a can-do attitude and willingness to learn
Desirable Experience/Qualifications:
• Experience with document control or technical documentation in a regulated industry
• Exposure to medical device regulations (EU MDR, UK MDR), ISO standards, or QMS
• Experience working across multiple departments or functions
Key Skills:
• Methodical and structured approach to work
• Strong prioritisation and multitasking skills
• Able to function effectively across interrelated departments
• High level of commitment and accuracy
• Ability to evaluate, interpret, and clearly present information