Regulatory Affairs Coordinator
1 week ago
About this role
We are seeking a talented Regulatory Affairs Trainee to join our team at GlaxoSmithKline. In this role, you will support the Regulatory Department in various activities, including dossier preparations, follow-up tasks, and system updates.
Key Responsibilities:
- Ensure regulatory correspondence files, trackers, and submission archives are up-to-date.
- Maintain regulatory databases by updating systems, trackers, and archives.
- Regularly update the MoHDT system to ensure compliance.
- Circulate incoming HA letters via the MoHDT system to responsible personnel.
- Support Veeva updates and assist in maintaining global and local regulatory databases.
- Assist in preparing MoH submissions, ensuring correct format and e-submission support.
- Collaborate with the regulatory department to maintain efficient regulatory archive management.
- Verify incoming HA letters in the EBS system if necessary.
- Check artwork components for regulatory compliance.
- Support the regulatory team in MM report preparations.
Qualifications and Skills
To be successful in this role, you will require:
- A minimum of 3 years of study in pharmacy or life sciences.
- Proficiency in computer skills.
- A good command of English.
- Strong communication skills.
- A willingness to work collaboratively as part of a team.
- An eagerness to learn through experience.
- The ability to work at least 3 days a week for a minimum of 6 months.
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