developed Providing support and guidance on technical, legal, and other issues as required Proactively working of OHSAS 18001, and ISO 14001 standards at the required time Undertaking 'active' monitoring and auditing bodies in the event of a major incident or as required Ensure accurate, comprehensive, and timely investigation suitability and workability of operational requirements and changes Monitor QA and FS Systems operation operation and make Additions, Changes etc as required Recruit and train suitable Staff in key positions to
students who are in their final year of study and require exposure to the work environment or have a prerequisite maintaining the Quality Management system. • Perform admin duties. • Assist in maintaining SABS ISO 9002/HACCP tertiary institution • A format for evaluation, required by the tertiary institution • Certified copies
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
monitoring and managing quality systems that support ongoing Laboratory Operations of specimen processing person in this position works on complex problems requiring data analysis and the ability to perform an in-depth Center Division. Project Management, coordination, support and implementation (30%) Communicate as needed (centralized laboratory data management system) support to sites; provide program input to the program developer, Frontier Sciences. Provide input and support to for HIV/AIDS Network Coordination (HANC) laboratory
monitoring and managing quality systems that support ongoing Laboratory Operations of specimen processing person in this position works on complex problems requiring data analysis and the ability to perform an in-depth Center Division. Project Management, coordination, support and implementation (30%) Communicate as needed (centralized laboratory data management system) support to sites; provide program input to the program developer, Frontier Sciences. Provide input and support to for HIV/AIDS Network Coordination (HANC) laboratory
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