to laboratory assistants (permanent and/or part-time) where and when applicable to the sample type and continuous improvement of laboratory and self by attending courses and doing literature studies. Improve application of ISTA and ISO/IEC 17025 in test aspects. Attendance of forums, congresses and seminars as recommended actions and laboratory. Liaison with the client/s. Attendance of Industry forums and congresses when recommended Responsible and supervising assistants (permanent or part-time) in sample handling and processing in relevant test
to laboratory assistants (permanent and/or part-time) where and when applicable to the sample type and continuous improvement of laboratory and self by attending courses and doing literature studies. Improve application of ISTA and ISO/IEC 17025 in test aspects. Attendance of forums, congresses and seminars as recommended actions and laboratory. Liaison with the client/s. Attendance of Industry forums and congresses when recommended Responsible and supervising assistants (permanent or part-time) in sample handling and processing in relevant test
to laboratory assistants (permanent and/or part-time) where and when applicable to the sample type and continuous improvement of laboratory and self by attending courses and doing literature studies. o Improve of ISTA and ISO/IEC 17025 in test aspects. o Attendance of forums, congresses and seminars as recommended and laboratory. o Liaison with the client/s. o Attendance of Industry forums and congresses when recommended Responsible and supervising assistants (permanent or part-time) in sample handling and processing in relevant test
Managing EHS site Managers & Labour training. Attending site meetings if required. Implementation &
improvements. Quantity and Quality: Achievements of timely submission and approvals in line with the registration HA guidelines and GRP, in the shortest possible time based on business priorities. License maintenance: Number of submissions in line with registration plan. Time to register new products vs. target and vs. industry submitted. Recording of risks in dossier at the time of submission. No disruption of stock supply as on outstanding responses to MCC recommendations. Attend local trade association meetings to network with
misses, create and close out action plans.
performance. Ensuring all products are manufactured in a timely and cost-effective manner. Qualifications and Requirements: manufacturing and QC Perform other duties from time to time as requested by the technical Manager General to optimize the process and to minimize process times for every stage and eliminate waste Evaluate raw and reduce dwell times Involved in all problem solving Analyze and product ‘First Time Right' report and simultaneously undertake tasks and projects to elevate ‘First Time Right' to target Review production schedules to
performance. Ensuring all products are manufactured in a timely and cost-effective manner.
Qualifications
manufacturing and QC
and create and closed out action plans.
meetings, forums and engagements