Advanced Medical Solutions is seeking a Regulatory Affairs expert to lead regulatory submissions for EU/US markets and global territories. You will maintain approvals, contribute to strategy, and oversee post-market surveillance activities to ensure ongoing compliance across product lines.
You will collaborate with Regulatory, Clinical, Quality, and Engineering teams, ensuring documentation, risk management, and audits are handled efficiently in a regulated environment.
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Regulatory Affairs Specialist - MedTech (EU/US) in Clive employer: Advanced Medical Solutions
Advanced Medical Solutions is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. With a strong focus on employee growth, you will have access to ongoing training and development opportunities while working in a field-based role that allows you to make a meaningful impact across NHS and private healthcare organisations in the UK.
Contact Details:
Advanced Medical Solutions Recruitment Team
