A leading medical device company is seeking a Regulatory Affairs Specialist for its office in Solothurn, Switzerland. The role requires supporting regulatory activities and ensuring compliance with Swiss regulations, with a focus on product registration and quality systems. Candidates should possess a Bachelor's degree, at least 2 years of experience in Regulatory Affairs or Quality Assurance, and proficiency in English and German. This hybrid position involves collaboration with various stakeholders and contributing to regulatory and quality improvement initiatives.
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