SE trainee SIVP:

The S Tunisia learner will be responsible for the post-approval changes dossier evaluation, preparation and dispatch to the countries for submission in line with local regulations and planning set up by Global/Regional BU/Country regulatory team.

Specific requirements and responsibilities include:

According to the country regulatory requirements and planning, assess, coordinate and contribute to the preparation of ready- to- submit regulatory dossier:Labeling, CMC, administrative, renewal /annual reportSite registrationTender

and /or any type of response documents to the Health Authorities questions by interacting with the relevant stakeholders (BU region regulatory, GRA, RSO local medical, local Pharmacovigilance department etc.) and monitoring of dossiers dispatch up to submission.

Ensure regulatory compliance with products overall strategies and  Health authorities country requirements evolutionBe compliant with all internal and external requirements, procedures and tools,Implement in timely manner Regional BU/country planning dispatch and ensure alignment with RA BU region and country activitiesMaintain a good working relationship with internal and external stakeholders, be a business partner for the BU/Country regulatory team  

Foster an environment/culture of learning and sharing of best practice within the team

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

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