Regulatory Affairs

1 day ago

Midrand, Gauteng, South Africa Novartis Full time R250 000 - R450 000 per year

Job Description Summary

To provide support to the RA department to ensure timely submissions and approvals of amendments in line with the submission plan and to meet regulatory objectives.

Job Description

Major accountabilities:

  • Understanding the Medicine Act and Pharmacy Act and the related Regulations and guidelines and how these influence the Regulatory Environment.

  • Understanding the elements of the Marketing Code.

  • Preparation and submissions of regulatory applications to SAHPRA.

  • Proof reading of artwork components.

  • Supporting compliance activities within the RA team

  • Being an active member of the RA team, participating in all team activities, meetings and gathering.

  • Support the RA team to meet its overall objectives.

Minimum Requirements:

Education:

  • Science degree with Honours or master's degree.

  • Exposure to Regulatory Sciences or experience in Regulatory Affairs will be an advantage.

Skills:  

  • Strong interpersonal and communication skills.

  • Highly organized.

  • Self-starter.

  • Ability to manage multiple projects and consistently meet deadlines.

NB: In order to be considered for the learnership:

  • Your application must be supported by a motivational letter and your academic transcripts

  • Must be a South African Citizen.

  • Ages between Years.

Languages :

  • English.

Novartis South Africa is committed to promoting equity (race, gender, and disability) through the filling of this post with a candidate whose transfer/promotion/appointment will promote representivity in line with the numerical targets as contained in our Employment Equity plan. While we are prioritizing designated groups, our selection process will still be based on the most suitable candidate, with the necessary skills and experience, as outlined in the job description.

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