Regulatory Affairs Scientist

About the position

Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies:

Key Responsibilities:

• Managing and coordinating the compilation and submission of new product applications.
• Managing and coordinating response to the regulatory authority.
• Maintain regulatory knowledge of the various territories where the registration process is required.
• Effectively managing, auditing and implementation of Regulatory systemsKey

Requirements:

• BSc or equivalent Science degree in a relevant field
• Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
• Demonstrable experience across the product development, commercialization, and life-cycle maintenance.
• Knowledge of new and emerging Acts, Regulations and Guidelines pertaining to the pharmaceutical [URL Removed] Competencies
• Sound project management skills
• Strategic thinking and planning
• Ability to handle multiple projects simultaneously.
• Cross Functional capability

(Full role profile available on application)

Apply to response "at" [URL Removed]

Subject: MP/AD_RAS

Supporting documentation required:
- Comprehensive CV
- Copy of Matric Certificate
- Copy of Tertiary Qualification

Desired Skills:

• Minimum 1-2 years' solid experience in Regulatory Affairs
• preferably in orthodox
• human medicines

Desired Work Experience:

• 1 to 2 years

Desired Qualification Level:

• Degree