A long-establihed leader in the pharmaceutical sector has an opportunity for an experienced regulatory affairs scientist, or senior regulatory affairs associate, to assist their experienced regulatory affairs pharmacist team. You need at least TWO full years of regulatory affairs scientist or regula
Monitor and retrieve all supplies and equipment. Make any solutions required for the laboratory . Properly dispose of any waste generated. Assist with lab clean-up and/or organi s ation. Write reports and provide plants etc. Catalog ue all equipment and chemicals. Make sure laboratory safety is maintained during experiments Biotechnology). An interest in science and technology backed up with sound mathematical skills and a practical hands
Monitor and retrieve all supplies and equipment. Make any solutions required for the laboratory . Properly dispose of any waste generated. Assist with lab clean-up and/or organi s ation. Write reports and provide plants etc. Catalog ue all equipment and chemicals. Make sure laboratory safety is maintained during experiments Biotechnology). An interest in science and technology backed up with sound mathematical skills and a practical hands
modification of formulas.
identification, modification of formulas. Coordinates scaled up plant manufacturing processes according to HSE and level as required. Reviews operational reports to make sure that quality standards, efficiency, and expenditure with Suppliers regarding technical matters and stays up to date with latest formulatory trends in the detergent achieved effectively. Able to evaluate progress and make appropriate adjustments to initial plans, ensuring
modification of formulas.
KPI reports. ▪ Ensure that product specs are kept up to date. ▪ Complete supplier questionnaires and renewals Results Oriented ▪ Good communication, decision making and interpersonal skills ▪ Strong presentation
intervals Ensure that all documents are controlled Make recommendations for further improvement/ development management with preventative recommendations and follow up on reports as required to ensure continual improvement information on the SHEMS to ensure effective and up-to-date information and submit SHE-related reports latest incidents and accidents to all team members – make sure all is recorded on attendance registers as
intervals Ensure that all documents are controlled Make recommendations for further improvement/ development management with preventative recommendations and follow up on reports as required to ensure continual improvement information on the SHEMS to ensure effective and up-to-date information and submit SHE-related reports latest incidents and accidents to all team members – make sure all is recorded on attendance registers as
be part of a dynamic team driving innovation and making a meaningful impact in the minerals processing za We appreciate that your CV might not be fully up to date. No problem just send us what you have. We