Responsible for the management of product portfolio and all aspects of marketing of Pharma products. MINIMUM a related field 3 – 5 years as a product/brand manager in a related field Digital marketing experience Pricing and price list Stock forecasting and management Corrective Actions Customer Liaison Maintain relationships Training of sales force Ensure Regulatory Compliance is adhere to Competencies: The ability & Organizing Passion for success Conflict Management Note: A Comprehensive list of all duties and
Marketing Manager - LVP Industry: Pharmaceutical Location: JHB Equity Requirement: EE Responsible for marketing strategies that drive top-line growth while managing the margins, enhance brand visibility, and increase equivalent qualification preferred Marketing / Brand management experience in the Medical/pharmaceutical Industry
an experienced product portfolio and marketing manager within pharmaceutical products provided to hospitals hospitals and clinics. Experience within pharma essential - other industry experience will not be considered sales data Budget and expense management Price and profitability management Customer liaison and quarterly future opportunities Compile monthly market reports Manage products complains and escalate to RP and Sales 5 years experience in pharmaceutical product management TBD Salary information is confidential
Product and Process Management
Regulatory Affairs Manager Industry: Pharmaceutical Location: JHB Equity Requirement: EE Lead the Regulatory ensure legal compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable) ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- and report other MRA's and third-party stakeholders Review regulatory agency submission of materials to ensure timelines accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission of new
Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services to control and manage a portfolio of product outputs. To ensure legal and regulatory compliance with with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines and Related ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work streams for- and report stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE EE Key Responsibilities: Manage work streams for- and report on the assigned portfolio of products Conduct with Regulatory Authorities, internal and external stakeholders Formulate or implement regulatory affairs systems, policies and procedures to ensure that regulatory compliance is maintained or enhanced. Key Requirements: Pharmacy Council 3 to 5 years' experience in Regulatory Affairs, preferably in human medicines Demonstrable
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical employ a Regulatory Affairs Scientist. The following applies: Key Responsibilities: Managing and coordinating applications. Managing and coordinating response to the regulatory authority. Maintain regulatory knowledge is required. Effectively managing, auditing and implementation of Regulatory systems Key Requirements: field Minimum 1-2 years' solid experience in Regulatory Affairs, preferably in orthodox, human medicines
looking for a Regulatory Affairs/Quality Assurance Pharmacist to join their team. Regulatory Affairs (RA): Assurance (QA): Assist QA Manager with artwork review and quality management system for Act 101 products release of Act 101 products in the absence of QA Manager and RP/Deputy RP. Review and update SOPs and Technical
A minimum of 8 years of pharmaceutical regulatory experience is a prerequisite with excellent knowledge
ensure legal compliance with the relevant Health Regulatory Authorities (Country Specific where applicable
relevant regulations in Africa.
Experience with regulatory authorities in sub-Saharan Africa and French
be advantageous
Significant experience of regulatory drug development, manufacture, commercialisation
commercialisation or equivalent.
Knowledge of regulatory procedures and legislation for drug development, product