Isheanesu Hungwe

Responsibilities: - Perform validation exercises in compliance with the cGMP standards and validation schedules. - Maintain compliant status of equipment and processes. - Development and implementation of a VMP that complies with the international standards regarding company`s processes and products. - Compile, maintain and update validation documentation as per SOPs and QMS. - Development of URS documents for manufacturing, Quality Control Laboratory and utilities. - Analytical instruments and critical utilities qualification and requalification (HVAC, Purified Water System and Autoclave). - Development and validation of analytical methods, manufacturing processes and cleaning methods for manufacturing equipment. - Evaluation of current analytical methods to improve and or introduce more efficient methods to improve laboratory productivity and reduce cost of analysis. - Participate in change control assessments to ensure compliant status of affected equipment is not compromised. - Adherence and participates in cGLP and cGMP personnel training. - Carrying out risk and impact assessment on systems. - Participates in internal, external (MCAZ and EU-GMP) and vendor audits. - Generate validation reports.

Responsibilities: - Perform validation exercises in compliance with the cGMP standards and validation schedules. - Maintain compliant status of equipment and processes. - Development and implementation of a VMP that complies with the international standards regarding company`s processes and products. - Compile, maintain and update validation documentation as per SOPs and QMS. - Development of URS documents for manufacturing, Quality Control Laboratory and utilities. - Development and validation of analytical methods for new products undergoing formulation research and existing products. - Qualification of new and existing equipment. - Critical utilities qualification and requalification (HVAC, Purified Water System, Water for Injection System and Autoclave). - Validation of new and existing manufacturing processes. - Validation of cleaning methods for manufacturing equipment. - Evaluation of current analytical methods to improve and or introduce more efficient methods to improve laboratory productivity and reduce cost of analysis. - Participate in change control assessments to ensure compliant status of affected equipment is not compromised. - Takes part in product registration and preparation of product dossiers. - Analysis of packaging, raw materials, in-process and finished products. - Handling and investigating market related complains. - Adherence and participates in GLP and GMP personnel training. - Carrying out risk and impact assessment on systems. - Participates product stability program and testing. - Participates in internal, external (MCAZ and SAZ) and vendor audits. - Mentoring of University students on industrial attachment. - Generate validation reports

Responsibilities: - Ensure efficient operation of the Quality Control Laboratory - Analysis of packaging, raw and in-process materials as well as finished products. - Schedule laboratory equipment servicing and calibrations. - Fertilizer blends formulation and development. - Generation of SOPs related to quality control and validation. - Develops and validates analytical methods for new products undergoing formulation research and existing products. - Qualification of new and existing equipment. - Validation of new and existing manufacturing processes. - Acting on capacity of the Production Manager (in case of his absence)

Responsibility: - Teaching Ordinary and Advanced Level Chemistry Students.

Responsibilities: - Carrying out calibration and maintenance of the laboratory instrumentation. - Perform instrumental and chemical tests for the elemental composition on geological, food products and water samples from different industries and institutions. - Research and development. - Standardisation of laboratory reagents and volumetric solutions. - Attending and reporting in brainstorming and progress report meetings (Stage Gate Meetings). - Report to the Research Scientist

Industrial Attachment