Job Description
A leading life sciences company in Switzerland seeks an experienced Regulatory Affairs professional to conduct regulatory impact assessments, manage registrations, and support FDA dossier preparations. The ideal candidate will have a Bachelor's degree, at least 4 years of experience in Regulatory Affairs specific to medical devices, and excellent communication skills, particularly in English. This role demands collaboration with global partners to ensure compliant submissions and regulatory requirements are met.
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Submit ApplicationJob Details
- Location Remote, Remote
- Job Type Full-time
- Category Other-General
- Posted Date June 22, 2026
- Application Deadline August 01, 2026