education and training: Diploma/Degree in General Nursing An Advanced Diploma in Midwifery would be advantageous Required minimum work experience: Minimum 1 year Nursing experience in a Maternal and Obstetric Unit (MOU) body registration: South African Nursing Council (SANC) in General Nursing Desirable additional education
Desirable
self-motivated and experienced Sugar Process Consultant, at middle management level, to join our dynamic industry. This will include the areas of industrial consulting, training, technology transfer, research and practical level. A proven track record in industrial consulting (preferably in sugar processing) and technology
self-motivated and experienced Sugar Process Consultant, at middle management level, to join our dynamic industry. This will include the areas of industrial consulting, training, technology transfer, research and practical level. A proven track record in industrial consulting (preferably in sugar processing) and technology
professional services of a Sustainable Design Consultant, with at least 2-3 years of successful private
professional services of a Sustainable Design Consultant, with at least 2-3 years of successful private
Please note that we are an immigration company and do charge a facilitation fee. We are accredited by OMARA, a branch of the Department of Immigration and Border Protection in Australia. For a Free Eligibility assessment please apply online, contact 27 21 201 1551 or follow the link to complete a fr
interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities for product portfolio. Support the collation interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities. Involvement in the development of Risk Management bid defence meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience
interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities for product portfolio. Support the collation interpretation of safety information collected from pre-clinical through to post-marketing, including medical requests on all drug safety matters from Regulatory Authorities. Involvement in the development of Risk Management bid defence meetings. Previous experience with authoring/reviewing PV procedures is preferred. Experience
mitigation plans in place to engage. Regulatory authorities when earliest signs of delay emerge. Proactively standards in the following process areas: Marketing Authorization Applications License maintenance e.g., Renewals Labelling and Artwork Management Robust Health Authority interactions To track and manage all GRP activities job profile. Marketing Authorization Applications: Submit Marketing Authorization Applications to the SA SA Health Authority according to SA HA guidelines and GRP, in the shortest possible time based on business