Role:Senior Principal Regulatory Affairs SpecialistLocation - Hampshire / HybridSalary-On applicationThis global company is currently looking for a highly motivated and talented individual with the following experience. This role is a management level role but will management projects rather than people.The role is hybrid and will be three days in the office. You must be based in the UK. For a full job description please do get in touchBelow is a summary of experience:8-12 years of experience in the regulated medical device industry. Extensive experience with regulatory submissions and technical documentation. Proven track record of managing complex regulatory projects and audits. Experience in electronic document management systems and RIMS– have the experience to navigate the electronic systems – Be tech savvy Would help if someone VEEVA experience. In-depth understanding of ISO 13485, MDSAP (Medical Device Single Audit Programme), MDD, MDR, and other relevant regulations. Not 100% a traditional regulatory role. It is a progressive role. (Hands on element needing to do registration activity ) Excellent attention to detail, organisational and technical writing skillsFor more detail on this role please get in touch with Julie Cooper at Mosaic Regulatory Solutions for a confidential chat.
