1.6 Store bulk and small sample rare red cells required for Reference Laboratory according to schedule Perform initial standardisation of rare reagents required for laboratory use. 1.10 Dispense rare reagents Screen for rare donations and crossmatch blood as required. 1.12 Confirm the phenotypes of donations placed Prepare various buffers and reagents as and when required. 1.16 Generate laboratory reports as designated review of root cause analysis and implementation of required corrective action within agreed timeframes. 2
1.6 Store bulk and small sample rare red cells required for Reference Laboratory according to schedule Perform initial standardisation of rare reagents required for laboratory use. 1.10 Dispense rare reagents Screen for rare donations and crossmatch blood as required. 1.12 Confirm the phenotypes of donations placed Prepare various buffers and reagents as and when required. 1.16 Generate laboratory reports as designated review of root cause analysis and implementation of required corrective action within agreed timeframes. 2
involved, including product release. Minimum Person Requirements Qualifications Experience Certification/ Professional least 2 years' experience in QA/QC type roles supporting commercial pharmaceutical operations Registration distribute any company product Quality system support: Assist with confirmation of implementation of partnerships. Define quality improvements plans to support continuous improvements to the contractor quality proposals from a quality and GMP perspective. Support submissions of accepted changes through regulatory
involved, including product release. Minimum Person Requirements Qualifications Experience Certification/ Professional least 2 years' experience in QA/QC type roles supporting commercial pharmaceutical operations Registration distribute any company product Quality system support: Assist with confirmation of implementation of partnerships. Define quality improvements plans to support continuous improvements to the contractor quality proposals from a quality and GMP perspective. Support submissions of accepted changes through regulatory
PA. KEY PURPOSE To ensure coordination of and support to the various quality, technical and document procedures, etc, as required by customers, sales orders, and business requirements. 2. Compile quality implementation and maintenance of various compliance requirements of the ISO quality system. 7. Monitoring, measuring completion of vendor / tender questionnaires with support from the relevant Departments. KEY COMPETENCIES spoken and written English. - Excellent customer support skills. - Good organisation and planning skills
Company and Client's products. This role will support the medical components of Pharmacovigilance (PV) Pharmacovigilance Practice and Regulatory Requirements. This role requires you to be a passionate pharmacovigilance and Clients. Support quality and efficiency strategies within the organization. Supporting the Business/ in the development of contracts and proposals. Supporting the Company by attending BID defence meetings meetings and conferences as the medical expert, as required. Providing Senior Management with regular updates
Company and Client's products. This role will support the medical components of Pharmacovigilance (PV) Pharmacovigilance Practice and Regulatory Requirements. This role requires you to be a passionate pharmacovigilance and Clients. Support quality and efficiency strategies within the organization. Supporting the Business/ in the development of contracts and proposals. Supporting the Company by attending BID defence meetings meetings and conferences as the medical expert, as required. Providing Senior Management with regular updates
making. Particular attention must be given to the requirements of the Integrated Coastal Management Act and company's role in providing scientific decision support and training to the Provincial authorities responsible Develop innovative applied research projects that support the needs of coastal communities, with a focus policy, providing scientific advice and decision support to national, provincial, and local government, management matters. Preferably a PhD, but a minimum requirement of a master's degree in environmental science
making. Particular attention must be given to the requirements of the Integrated Coastal Management Act and company's role in providing scientific decision support and training to the Provincial authorities responsible Develop innovative applied research projects that support the needs of coastal communities, with a focus policy, providing scientific advice and decision support to national, provincial, and local government, management matters. Preferably a PhD, but a minimum requirement of a master's degree in environmental science
making. Particular attention must be given to the requirements of the Integrated Coastal Management Act and company's role in providing scientific decision support and training to the Provincial authorities responsible Develop innovative applied research projects that support the needs of coastal communities, with a focus policy, providing scientific advice and decision support to national, provincial, and local government, The criteria Preferably a PhD, but a minimum requirement of a master's degree in environmental science