Join Zeda in Singapore! Attention Regulatory Affairs Specialists
As we scale our distribution network across Southeast Asia, we're on the hunt for new talent to help us navigate the regulatory landscape of medical device registration.
We Offer:
· A role within a small, dynamic team
· The chance to be part of something groundbreaking in the medical industry
· Opportunities to tackle diverse tasks and develop new skills
We Need:
· Singapore Citizen/PR mid-level professionals with experience in registering medical devices in Southeast Asia and working closely with health authorities during the review process
· Knowledge regarding local post-market regulatory requirements
· Attention to detail for maintaining the Regulatory Approval database
· Continued awareness of new legislation and policies impacting the product portfolio
· Individuals who value flexibility, are open to change, and are eager to learn
· Team players who are excited by the prospect of making a significant impact
· Experience in compliance or quality engineering highly regarded
This is a unique opportunity to contribute to a project that's not just exciting but also influential. If you're ready to step into a role where your work genuinely matters and can shape the future of healthcare in Southeast Asia, we want to hear from you!
Apply now and BUILD WITH US on our mission to revolutionise access to medical devices across the region.
