Regulatory Affairs Scientist
MVG Recruitment Specialists
- Undisclosed
- Permanent Specialist EE position
-
Johannesburg
- Posted 29 Apr 2024 by MVG Recruitment Specialists
-
Job 2562614
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:
Desired Qualification Level:
MVG Recruitment Specialists
About the agency
Headquartered in Cape Town.
Medical and Pharmaceutical Recruitment Specialists; Specialising in the placement of pharmacists, pharmacist assistants, nurses and technical staff into all areas of the medical/pharmaceutical industry nationally in South Africa. APSO Registered.
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