Working knowledge of global medical device regulations
Smith+Nephew is seeking a Regulatory Affairs Specialist to help ensure compliance and support regulatory submissions for their orthopaedics portfolio. The candidate will work in a hybrid environment and contribute to a collaborative team focused on medical device innovation
Job Summary
This role involves preparing global regulatory submissions including US 510(k) and EU technical documentation for the orthopaedics portfolio.
The company offers a collaborative global environment with flexible working models and comprehensive benefits including private health plans.
Success requires combining technical understanding with strong communication skills to support product changes and maintain compliance throughout the product lifecycle.
Matching Summary
Match Score: 85
Smith+Nephew is seeking a Regulatory Affairs Specialist to help ensure compliance and support regulatory submissions for their orthopaedics portfolio. The candidate will work in a hybrid environment and contribute to a collaborative team focused on medical device innovation.
Salary
Generous annual bonus; Pension schemes; Save As You Earn share options
Skills & Requirements
Must-have
Bachelor's degree in scientific or technical discipline