Technical Competencies & Experience:
Role Purpose
Development of procedures / test methods in relation to Epoxy testing and acceptance of raw materials, in-process, and final products in accordance Iso regulations. Conduct and develop new products research and development of raw materials and alternatives as well
Reference: JHB004977-KM-1 Well established East Rand based company seeks an R & D Manager with epoxy flooring experience Role Purpose Development of procedures / test methods in relation to Epoxy testing and acceptance of raw materials, in-process, and final products in accordance Iso regulation
Ref: LH 416494 - SENIOR R & D CHEMIST – EPOXY / CEMENTITIOUS APPLICATIONS Employer Description A industry. They are looking for a SENIOR R&D CHEMIST with at least 8 YEARS' R&D experience in the
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 Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work stakeholders Establish regulatory priorities and allocate resources and workloads Review regulatory agency submission accuracy, comprehensiveness, or compliance with regulatory standards Co-ordination and submission of new
Senior Regulatory Affairs Pharmacist Industry: Pharmaceutical Location: Midrand Equity Requirement: EE 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
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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) Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: Manage work 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
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
PE000998-CP-1 Our client is looking for an experienced Regulatory and Quality Assurance Pharmacist to join their experience Vet industry experience Knowledge of regulatory submissions in Botswana, Nambia, Zambia, Zimbabwe Job Duties Regulatory Affairs Duties Regulatory Submissions: Prepare and submit regulatory documents to comply with regulatory guidelines and requirements. Compliance: Monitor and interpret regulatory requirements registration of existing products. Coordinate with regulatory bodies for product approvals. Labeling and Advertising: