Role Summary:

Responsible for assisting the GE Healthcare regulatory team in gaining approvals and maintaining the regulatory compliance of the business. The role will primarily be involved in, but not limited to, the collection, organization and submission of information related to medical devices reports, corrections and removals, and other mandatory requirements for medical devices, as well as providing general administrative support to the regulatory team to facilitate regulatory services to the business.

Responsibilities:

1. Ensuring the accuracy and optimal presentation of information in submissions to regulatory authorities and internal presentations, and that they meet current best practice standards.

2. Liaising with relevant personnel within GEHC to ensure appropriate, timely input is provided for submissions to regulatory authorities and that all legally mandated deadlines for submission are met.

3. Providing administrative support to the regulatory processes, (i.e. compilation and dispatch of submissions, arranging payments to regulatory bodies).

4. Acting as regulatory functional expert in computer based support system in order to input, track and follow-up on information in the system.

Qualifications:

1. Master degree with pharmacy/medical background is preferred;

2. Good English reading and communication skill;

3. At least 3 days per week for 6 months.