Oluwayomi Akinmusire

Overseeing oil palm processing and production, ensuring efficient use of resources (raw materials, equipment, and labor). Monitor production metrics (yield, quality, throughput), Implementation of production schedules and meeting deadlines. Developing and implementing quality control measures. Manage product testing and certification. Schedule and overseeing maintenance activities. Managing equipment repairs and replacement and ensuring optimal equipment performance. Implementing safety policies and procedures by conducting regular safety audits with compliance with safety regulations. Managing emergency response plans for labor and production processes Coordinating raw material sourcing and overseeing logistics and transportation of material. Lead and motivate factory teams, Training and develop staff ensuring employee safety and well-being. Develop and manage factory budgets by monitoring expenses and optimizing costs. Analyze production data for process improvements. Implementing lean manufacturing principles. Foster positive relationships with local communities and managing community development projects. Preparing and submitting factory performance reports and maintaining accurate production records. Compliance with documentation regulations. Manage factory infrastructure and utilities. Ensuring security and access control, coordinating with other departments.

1. Operational use of Enterprise Resource Planning ERP for Approval of product, sales and planning 2. Documentation and verification of finished goods and Return Goods 3. Supervision of Good Document Practices 4. Environmental inspection, mapping and design 5. Annual Product Review and documentation of Products manufactured 6. Qualification of Bottel pack machine, labelling machine, autoclave, WFI plants, DM plants and Validation of SOP, Procedures and processes 7. Intravenous (IV) manufacturing, Oral Liquid and tablet manufacturing with In process control operations, supervision and documentation 8. Operation and documentation of Particle Counts and environmental mapping 9. Batch releases of IV, oral liquid and tablets with documentation 10. Tracking, trending, OOS and OOT identification, stability trends and compliance monitoring and CAPA review

Qualification of all old and newly acquired equipment and review quality outputs and change control Perform Quality Assurance document control function including document login, tracking, processing, distributing, BMR records and archiving of production related documents in compliance to internal and external requirements. Cordinate the revision, review of SOP - standard Operating Procedures and other GMP docuents Validation of cleaning process, manufacturing process and vendors (internal and external inspection) Common Technical Document (CTD) dossier officer, designing and submiting required documents to agency Designing protocols, documentation of performed process and participate in internal audits and supporting external audit Assist in Quality investigation, maintain change control and deviation processes for SOPs, master batch records, specifications, test methods, and other GMP documents. Training other employee on HSE related issues, documentation, process validation and equipment qualification process. In process quality control and analysis on manufactured products from liquids, tablets and packaging materials. Sampling and weighing of raw materials and documentation

Supervision, cordination and planning of process in the liquid drug manufacturing. Documentation and data integrity entry Analysis, adjustment and process deviations Process development, control and manufacturing cordination Training of staff and SOPs compliance monitoring Finished product approval and release for packing.

GLP complaince on line process checks, package intergity test, preparation of various chemicals for analysis, training of staff. cordination of comformity for preparation from raw material to finished good.