external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure Pharmacy Council -5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
experience of working in several groups in regulatory affairs or experience at a health authority
Knowledge
management of a skill group such as CMC, Regulatory affairs project management, etc.
Responsible
collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
experience of working in several groups in regulatory affairs or experience at a health authority Knowledge management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions
management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions experience of working in several groups in regulatory affairs or experience at a health authority Knowledge
management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions experience of working in several groups in regulatory affairs or experience at a health authority Knowledge
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
experience of working in several groups in regulatory affairs or experience at a health authority Knowledge management of a skill group such as CMC, Regulatory affairs project management, etc. Responsible for collaboration across the global, regional and local Regulatory Affairs interface enabling rapid and effective submissions
opportunity for an experienced regulatory affairs scientist, or senior regulatory affairs associate, to assist experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally, you should similar level to a pharmacist. Assist the regulatory affairs pharmacist team with all aspects of their
opportunity for an experienced regulatory affairs scientist, or senior regulatory affairs associate, to assist experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist scientist or regulatory affairs associate experience at a pharmaceutical company to apply. Ideally, you should similar level to a pharmacist. Assist the regulatory affairs pharmacist team with all aspects of their