continuous improvement Support production leads and operators for interpretation and methods following set standards according to the laid down procedures Ensure that all associated documentation is correctly completed according system Inspect all incoming goods and complete the associated paperwork according to the management system system Ensure that the laboratory and associated areas are kept clean and tidy and safe to work in Encourage Encourage quality awareness throughout the operation and reinforce the quality management system Support the
sector has an opportunity for an experienced RA Associate / RA Officer to assist the RA team. You need one one full year of RA Officer / RA Associate experience within the regulatory affairs department at a pharmaceutical experience as a Regulatory Affairs Scientist / RA Associate and/or RA Officer. A working knowledge of the have at least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company to apply
affairs scientist, or senior regulatory affairs associate, to assist their experienced regulatory affairs regulatory affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply at least 2 full years of RA Scioentist or RA Associate experience at a pharma company to apply. Salary
affairs scientist, or senior regulatory affairs associate, to assist their experienced regulatory affairs regulatory affairs scientist or regulatory affairs associate experience at a pharmaceutical company to apply at least 2 full years of RA Scioentist or RA Associate experience at a pharma company to apply. Salary
the Engineering Department.
Analyse risks associated with specific optimisation plans in terms of
performance measures.
Prepare consolidated operational reports on progress, performance and results
results of improvement projects.
Performing operational and time studies on processes within the production
candidate should possess hands-on operational expertise in Concentrator operations, adept at utilizing software experience working directly within concentrator plant operations as a Metallurgist, and proficiency in implementing minerals processing domain knowledge and its associated operational context to turn the Company's Level 3 analytics
manufacturing processes according to HSE and ISO operational protocols and applicable government regulations; at plant level as required.
manufacturing processes according to HSE and ISO operational protocols and applicable government regulations; training at plant level as required. Reviews operational reports to make sure that quality standards, functions within the role related to equipment operations, materials handling, as well as the safety of Main Working Relationships Internal Company Directors Laboratory Staff Plant personnel Procurement personnel
manufacturing processes according to HSE and ISO operational protocols and applicable government regulations; at plant level as required.
type roles supporting commercial pharmaceutical operations Registration with the South African Pharmacy periodically assess the overall quality risk associated to the contractor. Act on adverse trends to improve Stability: Ensure that the contract manufacturer is operating a Stability Surveillance program for Afrivet products type roles supporting commercial pharmaceutical operations Registration with the South African Pharmacy