At a Glance
- Tasks: Provide strategic input on regulatory requirements and prepare submissions for new technologies.
- Company: 1110 AD UK, a leading firm in Cambridge focused on innovative tech.
- Benefits: Competitive salary, opportunities for travel, and professional development.
- Other info: Strong project management skills needed; great career growth potential.
- Why this job: Join a dynamic team and shape the future of technology compliance.
- Qualifications: MS in Regulatory Affairs or related field, with FDA experience preferred.
The predicted salary is between 45000 - 60000 £ per year.
1110 AD UK in Cambridge is seeking a Regulatory Affairs Specialist to provide strategic input and technical guidance on regulatory requirements for new technologies. The role involves preparing submissions, interacting with regulatory authorities, and ensuring compliance with ISO 13485.
The ideal candidate will hold an MS in Regulatory Affairs or a related field, with experience in FDA regulations and a willingness to learn. Strong project management skills are essential, and the role may require some travel.
#J-18808-LjbffrWe think you need these skills to ace Strategic Regulatory Affairs Specialist – FDA & ISO 13485 in Cambridge
Regulatory Affairs
FDA Regulations
ISO 13485
Technical Guidance
Submission Preparation
Compliance Management
Project Management
