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: Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable
for over 5000 clients Reporting to Regulatory Affairs Manager Job purpose: Support the Regulatory team data gaps are addressed, in preparation for dossier call up and registration of complementary medicines and stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that
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: Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines Demonstrable
correspondence
- Formulate or implement regulatory affairs policies and procedures to ensure that regulatory
policy regulations
- Monitor regulatory affairs activities to ensure that they are aligned with
or green initiatives
- Monitor regulatory affairs trends that are related to environmental issues
development, commercialization and regulatory affairs, including conceptualization, design, and execution product development commercialization and regulatory affairs, including conceptualization, design, and execution development and commercialization and regulatory affairs Ability to collaborate remotely with team members
development, commercialization and regulatory affairs, including conceptualization, design, and execution product development commercialization and regulatory affairs, including conceptualization, design, and execution development and commercialization and regulatory affairs Ability to collaborate remotely with team members
products such as fragrance oils, personal care, home and fabric care product.
proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement
proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement