Role: Senior Principal Regulatory Affairs Specialist

Location: Hampshire / Hybrid

Salary: On application

This 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 manage projects rather than people.

The role is hybrid and will require three days in the office. You must be based in the UK. For a full job description, please get in touch.

Below 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; ability to navigate electronic systems – Be tech savvy. VEEVA experience would be advantageous.
• In-depth understanding of ISO 13485, MDSAP (Medical Device Single Audit Programme), MDD, MDR, and other relevant regulations.
• This role is not purely traditional regulatory work; it is a progressive role with a hands-on element involving registration activities.
• Excellent attention to detail, organizational skills, and technical writing skills.

For more details on this role, please contact Julie Cooper at Mosaic Regulatory Solutions for a confidential chat.