Sampling & analysis of co-products, effluent streams, equipment verification(TOC)and reagents preparation KHP standard for TOC and Reagents preparation Analysis of in process co-products; Germ, G20, G60 and
conferences (oral presentations).
flows on required process streams Conduct sieve analysis of raw materials on samples and manually record system daily Final Product Prepare samples for analysis, to ensure results are reported timeously and and the analysis thereof Prepare special samples to be shipped Communicate results of analysis to plant
Technician to join the team. Raw Material Do a sieve analysis of raw material sample on a daily basis and manually Do sieve analysis per unit and record results manually Communicate results of sieve analysis to Team Leaders/Production Prepare various raw material and product samples for analysis as instructed from time to time Grade 12 with
CT004297-OK-1 Pharmaceutical Client looking for a Senior Regulatory Affairs Pharmacist, to support the regulatory
manufacturing processes, ingredient and product analysis and verification, problem identification, modification with external company clients and suppliers at senior level. Ability to organise work program effectively
manufacturing processes, ingredient and product analysis and verification, problem identification, modification with external company clients and suppliers at senior level. Ability to organise work program effectively
with external company clients and suppliers at senior level
manufacturing processes, ingredient and product analysis and verification, problem identification, modification with external company clients and suppliers at senior level.