in performing accurate and timeous analyses on liquor samples. • Assist in implementing and maintaining
compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines applications for submission to the regulatory authorities Work in collaboration with internal and external maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate
the South African Health Products Regulatory Authority (SAHPRA) as well as the current guidelines and
the South African Health Products Regulatory Authority (SAHPRA) as well as the current guidelines and
obtaining and retaining environmental licenses/authorizations (WUL) Provide specialist input, relevant to compliance status of all permits, licenses and authorizations and facilitate implementation of corrective compliance status of all permits, licenses, and authorizations. Consult on the prevention and addressing of
obtaining and retaining environmental licenses/authorizations (WUL) Provide specialist input, relevant to compliance status of all permits, licenses and authorizations and facilitate implementation of corrective compliance status of all permits, licenses, and authorizations. Consult on the prevention and addressing of
OOS investigation and documentation experience. Author Environmental monitoring reports and review Microbiology
OOS investigation and documentation experience. Author Environmental monitoring reports and review Microbiology
Committees, South African Health Products Regulatory Authority and other regulatory bodies Ensure compliance
Committees, South African Health Products Regulatory Authority and other regulatory bodies Ensure compliance