Job Summary:Reviewing compliance level to ISO 9001:2015 Quality Manament Systems, implementing the perfomance improvement roadmap, and also developing certification plan for achieving the requirements of FSSC 22000: Food Safety Systems Certification.Specific Responsibilities:❖ Evaluating production process for compliance to QMS requirements.❖ Developing quality audit plans, audit reports, and audit follow-ups.❖ Identifying areas requiring training and the ensuring gaps are filled.❖ Collaborating with process owners for performance enhancement.❖ Identifying and correcting defections in the quality processes.❖ Inspecting and monitoring quality data for production processes.❖ Developing standards and procedures for operational processes.Accomplishments:Closed ten major non-conformities raised during the ISO 9001:2015 QMS re-certification audit, established effective QMS system for continual consistency, and developed an effective FSSC according to FSSC 22000.

Job Summary:Responsible for developing, implementing, and maintaining ISO 9001:Quality Management Systems, FSSC 22000: Food Safety Systems Certification, ISO 14001: Environmental Management Systems, and ISO 45001:2018 Occupational Health and Safety Management Systems (OHSMS) for producing high quality levels of Polyethylene terephthalate (PET) packaging products. Specific Responsibilities:❖ Assisting Regulatory projects that involve Quality Assurance oversight and inspection.❖ Manage product complaints, Corrective Actions and Preventative Actions.❖ Ensuring Quality Assurance aspects of warehousing practices in compliance with manuals.❖ Timely approve batches inspection and release according to LEO Standard Procedures.❖ Maintain appropriate documentation and ensured compliance to Good Manufacturing Practices.❖ Liaising with customers and regulatory authorities regarding quality audits.❖ Carried out all Standard Operating Procedures development, review, and implementation.❖ Conducted inspections of stakeholders as guided by the Good Manufacturing Practices.❖ Kept all the Company’s controlled and master document copies safe and confidential.❖ Conducted regular internal audits for continual quality system improvement of production.❖ Compiling information for procedures, instructions, forms, and other documents needed for the QMS.❖ Supporting implementation of specific procedures on request of Risk analysis and management.❖ Ensuring proper and effective product traceability, product recalls, and document retrieval.Accomplishments:❖ Developed an efficient and compliant Integrated Management System (IMS) for monitoring and controlling standards, effective risk analysis approaches, and operational excellence for consistency in Polyethylene terephthalate (PET) production and ensuring proper service delivery.

Job Summary:Was In charge of the Quality Control team for ensuring that fish production, processing and storage followed a set of quality assurance and food safety standards that maintains the integrity of the process, provides systems confidence, and ensures consistency in service delivery.Specific Responsibilities:❖ Held accountable for monitoring fish production process and quality check❖ Ensured hygienic and safety regulations are adhered to regarding OHS act.❖ Compiled timely, accurate, and complete results from customer surveys.❖ Monitored all aspects of production to ensure ISO 2200: FSSC and HACCP compliance.❖ In charged of reviewing the performance with pre-set ISO 9001:2015 standards.❖ Prepared quality manuals and update them at regular basis as required.❖ Coordinated periodic inspections of the premise by regulatory authorities.❖ Ensured proper waste management and pest control within the premises.❖ Supported the induction and training of new production personnel.❖ Was a key member of the internal audit team; organize internal and external audits for QMS.❖ Ensured documentation of the QMS programs were very organized and easily retrievable.❖ Ensured that all procedures along the chain were in place for customer requirements and audits.❖ Provided full assessment on management systems compliance to quality and food safety systems.Accomplishments:❖ Developed an automated dashboard system based on well-defined metrices and cloud-configured programs for information management system (IMS). This led to instant scale up of the company operations and planning that further elevated returns in terms of sales.

Job Summary:Supported KEMRI-CDC HIV-Research Laboratory in performing HIV-1 sub-types recombination and genotyping to detect specific genetic mutations HIV in patients with antiretroviral therapy (ART) treatment failures as well as assessing patient prognosis by monitoring the effects of antiretroviral therapy (ART) on the HIV-1 viral load.Specific Responsibilities:❖ Supported validation of lab reagents, protocols, and new equipment.❖ Ensured proper logging of Lab samples into the master laboratory log.❖ Supported laboratory performance testing using samples provided.❖ Prepared calculation of control limits, detection limits, for lab analyses.❖ Provided technical expertise on experimental design, and optimization.❖ Prepared, reviewed, and updated the Lab Chemical Hygiene Plan.❖ Maintained relevant online databases, document filing systems, and reagents inventory. ❖ Supported in Ensuring optimal management of the PRECISE study biorepository within the La.❖ Performed relevant sample analysis, including DNA Extraction, ELISA, PCR, and Sequencing.❖ Submitted complete progress reports on a timely fashion as scheduled by the management.❖ Took minutes during meetings in the absence of the laboratory supervisor.Accomplishments:❖ Was an active team member in leading the Lab towards getting Virology Quality Assurance approval for Integrase Genotyping methods using plasma in patients failing third line antiretroviral therapy (ART) regimens as well as acquiring WHO accreditation culminating towards the Lab nomination as a Regional reference Lab for HIV-1 Genotyping in East Africa.