We are the Global leader in eye care and have built a rich history of providing innovative products to customers and patients all over the world.
Job Description This internship provides an introductory platform to medical device regulations in Asia Pacific. Being part of the Regional Regulatory Affairs team based in Singapore, the intern is able to understand the significance of regulatory approvals for commercial activities in countries and how internal stakeholders across different departments work together to ensure the delivery of quality and regulatory approved medical devices to patients at the end of the day.
This intern will support the Regional Regulatory Affairs team in regulatory affairs operation tasks across Asia Pacific. The responsibilities include:
- Review of Global Regulatory Registration Database and ensure the regulatory data is aligned with Asia country data
- Consolidate supply chain codes with registration information in regulatory database
- Prepare country renewal requirements for 2020 and 2021 by Q3 2019
- Maintain countries registration trackers
- Consolidate and maintain regional monthly dashboard
- Other operation tasks and projects as assigned
Requirements: - Undergraduate students in faculty of Pharmacy, Science or Biomedical Engineering
- Minimum 3 months full time internship starting Aug 2019; open to school placement internship program starting Aug 2019.
- Prior internship experience is a plus
Application Instructions
Please apply for this position by submitting your resume (with email address, contact details and internship availability period) using InternSG.
Kindly note that only shortlisted candidates will be contacted.
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