Global Regulatory Expert
At our international company, we're on the lookout for an accomplished Regulatory Affairs Manager to lead our global product registrations in Latin America. As a trusted expert, you will spearhead regulatory projects from development through implementation.
This pivotal role demands a deep understanding of international regulations and laws. Your analytical mindset, coupled with hands-on expertise, ensures seamless project execution. A keen eye for emerging regulatory requirements guarantees smooth operations.
We're seeking someone who excels at coordinating, planning, and testing critical documentation. University graduates or diploma holders in natural sciences are preferred, alongside relevant work experience in international medical device registration. Proficiency in English and German is essential; additional language skills, particularly in Spanish or Portuguese, are valued assets.
* A degree in natural sciences or a related field;
* Experience in international medical device registration;
* Proficiency in MS Office and regulatory submissions;
* Excellent command of English and German languages, with other languages (especially Spanish, Portuguese) being advantageous;
In this challenging yet rewarding role, you'll contribute to the development of innovative medical devices that improve patients' lives worldwide. We prioritize your work-life balance and offer individualized career advancement opportunities through our L&R Academy.
Quality and Regulatory Affairs | Neuwied