Job Title: Regulatory Affairs Pharmacist Location: Johannesburg, South Africa Industry: Pharmaceutical Regulatory Affairs Pharmacist to join their team in Johannesburg. The Regulatory Affairs Pharmacist will Minimum 2-3 years of experience in regulatory affairs within the pharmaceutical industry Knowledge of
Job Title: Regulatory Affairs Pharmacist Location: Johannesburg, South Africa Industry: Pharmaceutical Regulatory Affairs Pharmacist to join their team in Johannesburg. The Regulatory Affairs Pharmacist will Minimum 2-3 years of experience in regulatory affairs within the pharmaceutical industry Knowledge of
for over 5000 clients Reporting to Regulatory Affairs Manager Job purpose: Support the Regulatory team stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that
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
Required minimum work development and commercialization and regulatory affairs
instrumentation in either: chemistry, biochemistry, water testing, or pharmaceutical sciences. The focus will experience in a lab environment using chromatography Water testing laboratory experience APPLICATION INFORMATION
instrumentation in either: chemistry, biochemistry, water testing, or pharmaceutical sciences. The focus will experience in a lab environment using chromatography Water testing laboratory experience APPLICATION INFORMATION
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 business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
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 business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved