methodology. Promoting and maintaining laboratory safety procedures at the section level. Promoting and efficient laboratory conditions required for personnel safety and effective running of tests. Providing guidance
methodology. Promoting and maintaining laboratory safety procedures at the section level. Promoting and efficient laboratory conditions required for personnel safety and effective running of tests. Providing guidance
RA Associate / RA Officer to assist the RA team. You need one full year of RA Officer / RA Associate experience Regulatory Affairs Scientist / RA Associate and/or RA Officer. A working knowledge of the South African Health ethics. MUST have at least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company
clinical data appraisals Always keeping the end-user/ safety of patient in mind Ability to develop good working
clinical data appraisals Always keeping the end-user/ safety of patient in mind Ability to develop good working
overall performance of the department and company. Safety Management, Quality control, Quality Assessment Technologist preferred. • Experience in clinical safety laboratory management, PBMC (peripheral blood mononuclear
overall performance of the department and company. Safety Management, Quality control, Quality Assessment Technologist preferred. • Experience in clinical safety laboratory management, PBMC (peripheral blood mononuclear
areas, workstations, and equipment. Comply with safety rules and regulations. Comply with laboratory dress pharmaceutical industry is preferred. Good understanding of Safety and cGMP practices Computer Literacy Market Related
areas, workstations, and equipment. Comply with safety rules and regulations. Comply with laboratory dress pharmaceutical industry is preferred. Good understanding of Safety and cGMP practices Computer Literacy Market Related
skills. - Computer savvy, particularly with MS Office suite.