Requirements: English
Company: switzerland.xpatjobs.com
Region: Solothurn Canton
We are currently looking on behalf of one of our important clients for a Regulatory Affairs Specialist. The role is a permanent position based in Solothurn Canton.Your Role: Prepare product approval documents for medical devices with authorities worldwide. Supervise development projects regarding regulatory affairs. Assess amendments. Negotiate contracts with customers regarding Regulatory Affairs aspects. Correspond & communicate with authorities. Assist in customer & authority audits according to ISO 13485 & 21 CFR 820. Carry out general QM tasks such as training & the creation of associated documents.Your Skills: At least 5 years of professional experience in Regulatory Affairs, including experience with a focus on Medical Devices. Any experience in relation to Software & Interactive Medical Products is very advantageous.Your Profile: Completed University Degree in Natural Sciences / Engineering or equivalent training. Highly motivated, responsible, quality-aware, customer-oriented & communicative. Fluent in English (spoken & written), any German language skills are considered a strong plus.If you wish to apply, please send us your resume in Word format with some references.You can also register on our website which will allow you to receive other exclusive and confidential job offers.