Senior Regulatory Affairs Executive [Device / MNC / CE Mark]

Partnering with a Medical Device MNC with an established branding, our client is seeking a Senior Regulatory Affairs Executive as part of their expanding setup in Singapore. Reporting to the Senior Regulatory Affairs Manager, we are looking for someone with good knowledge of regulatory framework in Singapore. In this position, you will prepare technical dossiers for submission to Europe (CE Mark) and US FDA (510K) and also work closely with regional affiliates to help them obtain product approval. You will be responsible for ensuring compliance with regulatory requirements, maintaining accurate records, and staying up-to-date with regulatory changes. This is a fantastic opportunity to join a leading Medical Device company and contribute to the development of innovative products that improve patient lives. If you are a motivated and detail-oriented professional with a passion for regulatory affairs, we would love to hear from you. Please submit your application, including your CV and a cover letter, to [insert contact information].