* Implement programs and procedures to effectively evaluate, monitor and trend product quality. * Ensure that all raw material requirement for the factory is at the correct quantity and quality aimed at continually Production without negatively affecting Equipment Utilization.*Ensure prompt attention of Site Leadership Team in areas of risk, pertinent to quality, Manufacturing and Production as they arise during plant operations, which may have an adverse effect on Food Quality, Safety, Operations and Supply.*Support and contribute to strategies for assessing site GMP and Implementation to ensure compliance with industrial standards - ISO 9001:2015,Fssc 22000 V 5.1 and Halal Certification System*Supports manufacturing operations (upstream and downstream) to deliver Operational Efficiency and Production Output.* Review documentation associated with production operations. * Ensuring that adequate level of documentation acceptable and compliant to existing procedures and adopted Standards from ISO 9001:2015,Fssc 22000, V5.1 and Halal Certification Systems are in Place and in Use.* Participates in activities associated with event resolution and CAPAs with a focus on organizing and attending cross-functional meetings.*Writes, reviews and seek approvals for Standard Operating Procedures (SOPs), when required.*Supports operations to encourage a Quality Culture, Operational Efficiency, and a safety on Site.* Identify Bottlenecks in Quality Management systems, Operational Efficiency to Drive Continuous Improvement.*Assist where applicable for safety, Environmental and quality trainings to Team as stipulated. *Ensure compliance with State and Federal regulatory agencies as it relates to Quality, Product, and environmental safety.

* Driving Compliance to quality norms, policies, and Procedures. * Co-ordinate and supervise packing, loading and dispatch activities.* Ensure adherence to HSE and Food Safety standard and ensure safe working environment.* Manage staff for teamwork and effectiveness Lead good manufacturing and hygiene practice.* Handle Stock control and reconciliation of raw materials ,for plant daily operation.* Support with trials for product improvement and implementation of new products with adequate understanding of Artwork Design and Control, Equipment Qualification, and Process Validation.* Resolve work problems and recommend measures to improve productivity, in a bid reduced Consumer Complaints by < 0.1* Ensure adherence to safety regulations and laid down policies and procedures with Zero Accident Hours.* Performed any other duties that may be assigned by head of Quality.

* Ensures existing documentation is in accordance with established documentation procedures/regulatory compliance requirements.*Documentation includes lot code calendars, production batch records (BR), standard operation procedures (SOPs), logbooks, production checklist, daily inspections.*Ensuring the maintenance of all approved cGMP production documentation.*Oversight of finished goods release after review of related documentation and products for all OTC drug and dietary supplement products. Ensure product integrity, accuracy, efficacy and labeling meets standards; Creating and issuing all COA’s to customers where required.*Issue Batch Records and Production labels*Determine quality status of raw materials, finished product, quarantine material, and production holds.*Entering disposition of finished goods product in the inventory management system*Daily supervisory tasks of all QA technicians. Tasks including vacation approval, attendance, reviews, multi-purpose forms, disciplinary actions, and ensure training requirements are met.*Support Process validation activities*Performs other duties as required

*I ensure Risk Management Process for process and system failures by participating in RCA, deviation and risk assessment meetings and ensuring full approval of actions before implementation.*Supervision and driving of all Quality and Food Safety Improvement initiatives and measures to achieve effective operations of Tetra, PET and CAN lines.*Drive product artwork control to ensure all content on printed product packaging components is correct and in accordance with registered details, or label claims/requirements.*Ensuring that new equipment and processes are validated before use and ensure continuous validated state throughout their life cycle. *I ensure Risk Management Process for process and system failures by participating in RCA, deviation and risk assessment meetings and ensuring full approval of actions before implementation.*Auditing standard operating procedures and other sections within the company, ensuring conformance to standards, ISO 9001, FSSC 22000 and regulatory requirements.*I Develop SOPs, related documents and implementation of appropriate procedures in line with SBFE standards to ensure all products meet stipulated Quality and Food Safety standards making them fit for human consumption.

*Performed efficient and world-class physical and chemical analytical evaluation of all Finished product, Raw and intermediate materials to reflect their true quality integrity in accordance with GSK requirement and other international compendia (USP, BP, Ph Eur., etc).*Developed, review and implement all Finished Products testing procedures and related documentation in accordance with GSK global requirements for ensuring total compliance to GSK’s Quality Management System (QMS).*Participated in efficient and effective physico-chemical analytical evaluation of all counterfeited and suspected fake product for Regulatory Affair/Legal department for required disposition and Legal action.*Providing adequate technical trouble shooting support of laboratory equipment to forestall product releases delay/recall due to unreliable analytical data as a result of faulty equipment.*Implemented all EH&S directives on the use of work environment, tools, materials and products to ensure safety at workplace.*Adherence to Good Laboratory Practice (GLP) in order to maintain world-class laboratory operations.*I undertook general audit of production processes, equipment and products (intermediate and finished) in compliance with Good Manufacturing Practice (GMP), GlaxoSmithKline Global Quality Policies (GQP) and National Regulatory Standards for Pharmaceutical production, to ensure consistent quality of products from batch to batch.*I ensured withdrawal of retain samples for storage to ensure representative retention of Products before the expiration of such products and ensure retrieval of both retained samples and batch records in record time in compliance with GMP expectations on documentation.*I undertook general Quality Inspection of finished goods/raw materials warehouse and other storage rooms to ensure finished Goods/Raw Materials are kept at specified storage conditions

●Elected as Corpers Liaison officer, Agbara branch to co-ordinate, Manage and protect the integrity and rights of corp Members. ●I demonstrated the ability to work independently, under pressure at tight deadlines.●I demonstrated strong ability to take evidence – based decision making Capabilities with excellent communication skills.