The common responsibilities for this position include managing regulatory submission and approval in collaboration with local and global teams to ensure timely product listings. Additionally, the role involves submitting technical documentation to the Department of Health for new or changed listing applications of medical devices. The intern is also responsible for maintaining the Regulatory Affairs (RA) database and providing local and global RA teams with real-time information necessary for maintaining key metrics, including submission and approval dates for all medical device listings.
The percentages next to each skill reflect the sector’s demands in these respective skills. E.g., 30% means this skill has been listed in 30% of all the job postings in this sector.
The skills distribution tells you what specific skill sets are in demand. E.g., Skills with a distribution of “More than 50%” means that these skills are wanted in more than 50% of the job postings.
Types of companies in the sector that have advertised a position
Education level required as indicated
Fields of study of the positions advertised by employers
Employment Mode of the positions advertised by employers
Employment Type of the positions advertised by employers