direct responsibility for the deliverable of the Market Shaping output, manage all milestones, timelines interdependencies Lead the implementation of the Market Shaping working Location: Parktown – Johannesburg Provide overall project leadership of market surveillance Develop market shaping strategy and detailed annual and lead deal design Identification and design of market-shaping interventions Oversee the development of stakeholders Lead and coordinate implementation of the market-shaping output Develop and maintain a strong relationship
direct responsibility for the deliverable of the Market Shaping output, manage all milestones, timelines interdependencies Lead the implementation of the Market Shaping working Location: Parktown – Johannesburg Provide overall project leadership of market surveillance Develop market shaping strategy and detailed annual and lead deal design Identification and design of market-shaping interventions Oversee the development of stakeholders Lead and coordinate implementation of the market-shaping output Develop and maintain a strong relationship
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: Managing and coordinating the compilation and submission of new product
requires. Ensure release of 3" party products on time. Sends relevant QA reports to contract givers for responded to by the QMS officer. Assist with marketing and regulatory affairs. Functions Assists QA Manager
registered with SAVC as a Veterinary Technologist (not student registration).
stay updated on product developments, conduct market research, spearhead product development, and manage training sessions and presentations •Market Research: Conduct thorough market research to recognize industry tailor our offerings to meet customer demands •Market Awareness: Develop strategic plans to identify multiple projects concurrently and ensure their timely completion Key Requirements: Bachelor's degree ability to effectively prioritize tasks and manage time; willingness to travel locally and internationally
the RA Manager and cross functional team and marketing teams on the regulatory submission progress of improvements. Quantity and Quality Achievements of timely submission and approvals in line with the registration with international priorities and local brand marketing strategy. On-going proactive identification and GRP standards in the following process areas: Marketing Authorization Applications License maintenance relevant to job profile. Marketing Authorization Applications: Submit Marketing Authorization Applications
the RA Manager and cross functional team and marketing teams on the regulatory submission progress of improvements. Quantity and Quality Achievements of timely submission and approvals in line with the registration with international priorities and local brand marketing strategy. On-going proactive identification and GRP standards in the following process areas: Marketing Authorization Applications License maintenance relevant to job profile. Marketing Authorization Applications: Submit Marketing Authorization Applications
Sub-Saharan Africa cluster and as required by Marketing Authorization Holders (MAH) and/or study sponsors supporting the needs of the local Medical and Marketing organization in collaboration with the International Reports (PSURs/DSURs), as applicable, Plan and ensure timely submission of Aggregate Reports according to local Support LSO/CSTL in the preparation, conduct and timely documentation of Pharmacovigilance training for contributions and data, as needed, accurately and in a timely manner. Responsible for the local PSMF implementation
Sub-Saharan Africa cluster and as required by Marketing Authorization Holders (MAH) and/or study sponsors supporting the needs of the local Medical and Marketing organization in collaboration with the International Reports (PSURs/DSURs), as applicable, Plan and ensure timely submission of Aggregate Reports according to local Support LSO/CSTL in the preparation, conduct and timely documentation of Pharmacovigilance training for contributions and data, as needed, accurately and in a timely manner. Responsible for the local PSMF implementation