Quality Assurance Pharmacist ensures that Company Products comply with the local and international Quality assurance function throughout the processes involved, including product release. Minimum Person Requirements qualification: Spearhead the vendor selection process according to company SOPs; conduct vendor inspection test, and warehouse or distribute any company product Quality system support: Assist with confirmation contractor quality compliance. Change control: Assess product related change proposals from a quality and GMP
Quality Assurance Pharmacist ensures that Company Products comply with the local and international Quality assurance function throughout the processes involved, including product release. Minimum Person Requirements qualification: Spearhead the vendor selection process according to company SOPs; conduct vendor inspection test, and warehouse or distribute any company product Quality system support: Assist with confirmation contractor quality compliance. Change control: Assess product related change proposals from a quality and GMP
Quality Inspections: 3. Co-ordinate and facilitate product and equipment quality related inspections with action processes. Quality Document Control: 10. Document co-ordination, liaison and processing between between Process Automation and customers. 11. Updating customer document portals and vendor compliance portals required. - Good knowledge and understanding of PA products and equipment required. - Good knowledge and experience
the regulatory submission progress of specific products and ensure support needed to drive performance Practice (GRP) Ensure that all the regulatory processes are performed timeously and in line with GRP. Maintain GRP standards in the following process areas: Marketing Authorization Applications License License maintenance: Ensure all post-approval product maintenance activities including CMC variations through the Company. Global Labelling Business Process using the GAZELLE system. Co-ordinate the operations
Principals, and to control and manage a portfolio of product outputs. To ensure legal and regulatory compliance South African Pharmacy Council, ensuring timeous processing of regulatory applications. Key Responsibilities: on the assigned portfolio of products: Assisting with internal product queries from relevant departments departments Assisting with external product queries from the SAHPRA, other MRA's and third-party stakeholders standards Co-ordination and submission of new product applications in South Africa and other applicable
stakeholder engagement and client management. Core product/service development and implementation Compilation Compilation and implementation of the company's core products and services (specialising in no less than three): Stakeholder Engagement (including Public Participation Processes) Baseline Socio-Economic Study Surveys Social reporting Undertake qualitative (issues based processes) and quantitative (survey) research, data analysis Stakeholder Engagement Undertaking public participation processes, stakeholder engagements and community consultations
stakeholder engagement and client management. Core product/service development and implementation Compilation Compilation and implementation of the company's core products and services (specialising in no less than three): Stakeholder Engagement (including Public Participation Processes) Baseline Socio-Economic Study Surveys Social reporting Undertake qualitative (issues based processes) and quantitative (survey) research, data analysis Stakeholder Engagement Undertaking public participation processes, stakeholder engagements and community consultations
coordinating the compilation and submission of new product applications. Managing and coordinating response the various territories where the registration process is required. Effectively managing, auditing and human medicines Demonstrable experience across the product development, commercialization, and life-cycle
coordinating the compilation and submission of new product applications. Managing and coordinating response the various territories where the registration process is required. Effectively managing, auditing and human medicines Demonstrable experience across the product development, commercialization, and life-cycle
packaging material, raw material, finished bulk and product release testing as well as manage and supervise materials, packaging materials, labeling and finished products that are non-conforming. Liaise with suppliers provide technical service to problems arising in production. Provide technical support for Manufacturing Implement improvements to production processes that lead to overall increases in product quality. Approve/reject to assure quality before incorporation into the product. Ensure quality checks of all incoming raw material