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Mvg Recruitment Specialists JohannesburgRegulatory Affairs Specialist · A large pharmaceutical manufacturing facility is seeking a highly skilled Regulatory Affairs Specialist. · Key Responsibilities: · To manage and coordinate the compilation and submission of new product applications, ensuring compliance with relevan ...
- Eli Lilly and Company Johannesburg
At Eli Lilly and Company, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need ...
- Compile and submit new product applications in accordance with regulatory requirements.
- Cultivate strong relationships with regulatory authorities through effective communication and submission of responses.
- Stay up-to-date on regulatory knowledge across various territories requiring registration.
- Manage, audit, and implement robust regulatory systems ensuring compliance and efficiency.
- Bachelor's degree in a relevant science field or equivalent qualification.
- A minimum of 1-2 years' experience in Regulatory Affairs, preferably in human medicine.
- Demonstrable experience spanning product development, commercialization, and life-cycle maintenance.
- In-depth knowledge of emerging Acts, Regulations, and Guidelines impacting the pharmaceutical industry.
- Strong project management skills and ability to think strategically.
- Effective multitasking and cross-functional capabilities.
Regulatory Affairs Scientist - Johannesburg - MVG Recruitment Specialists

Description
Regulatory Affairs Specialist Role
We are seeking a Regulatory Affairs Scientist to join our team at a large pharmaceutical manufacturing facility.
The following key responsibilities will be expected:
To excel in this role, the ideal candidate will possess the following qualifications:
Please refer to the full role profile for additional information.
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