Regulatory Affairs Intern
You are responsible for:
- Compile the Regulatory documents for the related stakeholders and as per local regulations.
- Review local artworks and materials as needed in local language.
- Support in the notification process with local authorities for medical devices as applicable.
- Review local regulatory related procedures in markets as needed and gather the information from the team to propose the final comments.
- Supporting the assessment of documentation to meet in-country local requirements.
- Supporting in compiling local in-country documentation and /or follow-up with in-country regulatory and legal manufacturers /business units regulatory team.
- Support in building databases with completion and review.
To succeed in this role, you would require a customer first attitude and the following:
- Perusing Bachelors/Master's (engineering background preferred)
- Able to complete 6 months for the internship.
- A team player with positive attitude and eagerness tolearn.
- Good communication skills, both oral and written.
- Sharp eye to detail
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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