Senior Regulatory Pharmacist. Job Purpose: Support the Regulatory team to provide superior Regulatory services To ensure legal and regulatory compliance with the relevant medicine Regulatory Authorities (Country processing of regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned of products: Assisting with internal product queries from relevant departments Assisting with external stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE Responsibilities: Manage work streams for- and report on the assigned portfolio of products Conduct dossier 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
implement analytical tools to ensure accurate reporting.
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) processing of regulatory applications. Key Responsibilities: Manage work streams for- and report on the assigned of portfolios Assisting with internal product queries from relevant departments Assisting with external other MRA's and third-party stakeholders Review regulatory agency submission of materials to ensure timelines
Regulatory Affairs Scientist Industry: Pharmaceutical Location: JHB Equity Requirement: EE Large Pharmaceutical Pharmaceutical Manufacturing facility seeks to employ a Regulatory Affairs Scientist. The following applies: Key coordinating response to the regulatory authority. Maintain regulatory knowledge of the various territories Effectively managing, auditing and implementation of Regulatory systems Key Requirements: BSc or equivalent Science 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): including database maintenance. Quality Assurance (QA): Assist QA Manager with artwork review and quality management the QMS. Co-audit local audits, generate/review reports, and close findings via CAPA. Log and follow up stability reports, update stability logs, and notify the Responsible Pharmacist (RP) of findings. Assist with required. Prepare for inspections, renew licenses, and assist with GMP in-house training. Act as an authorized
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
relationships effectively and provide required regulatory support. Reviewing artwork relating to products abreast of developments and changes in the local regulatory environment which directly impacts on the product Council (SAPC) is essential Minimum of 2 years Regulatory Affairs experience in pharmaceutical industry industry . Experience working with SAHPRA and other Regulatory Authorities in Africa. Excellent spoken and written In-depth knowledge of regulatory requirements . Understanding of regulatory compliance and the impact
Responsibilities:
Reporting Administrator – Centurion, Pretoria / Tshwane. Company Name: Service Solutions. Position Level: services of a reporting administrator whose main responsibility will be to compile ad-hoc reporting, and report compile reports, derived from our Telematics Solutions on a daily basis and generate ad hoc reports when when required. The reporting administrator role includes reporting on, following up with customers and manage