The ideal candidate will have experience in the medical devices industry and a deep understanding of regulatory affairs and compliance.

Responsibilities include:

• Assist in coordinating/preparing and reviewing regulatory submissions for Delta’s products and following up on customs clearance whenever needed.
• Keep track of the progress of regulatory submissions to Complete regulatory submission forms within the assigned time frame.
• Handling all medical device related communications
• Coordinating the paperwork between suppliers and EDA
• Ensuring compliance with all necessary regulations
• Maintain adequate records for suppliers documents.