Experience

• 

  Neimeth int. pharmaceuticals plc. lagos state

  Jul 2010 - Oct 2012

  Gmp coordinator

  As a GMP Coordinator, I managed key activities to ensure strict adherence to GMP standards and operational efficiency. My responsibilities included overseeing product sampling, conducting internal audits, maintaining comprehensive documentation, performing periodic product reviews, and ensuring continuous water quality monitoring and general housekeeping.I also directed manufacturing scale-up processes, which involved generating, reviewing, authorizing, and archiving critical processing and testing documentation. These efforts supported seamless production transitions and ensured full regulatory compliance throughout the manufacturing cycle.* Enforced GMP compliance throughout manufacturing by monitoring deviations, managing CAPA, and developing Standard Operating Procedures (SOPs) both independently and in collaboration with cross-functional teams.* Coordinated and executed the nationwide supply and delivery of over 100 drug products per centre/state for a multimillion-naira Federal Government drug order, achieving 100% delivery accuracy with zero reports of missing items or quality defects.* Designed and delivered comprehensive training programmes for new hires and ongoing staff development, resulting in high-performing employees frequently recruited by competitors due to their advanced skill sets.* Earned commendation from WHO Technical Assistance Programme consultants during audit evaluations for consistently upholding high-quality standards and compliance. Show less

• 

  Neimeth international pharmaceuticals plc.

  Nov 2012 - Aug 2023

  As a part of this job role, I worked with the Executive management to direct corporate strategy execution, focusing on organizational restructuring and improving operational efficiency to stabilize and grow the business. I worked closely with board members and senior leadership to achieve business objectives, strengthen governance practices, and address operational risks.Additionally, I participated in financial restructuring initiatives and cost control measures that kept the company afloat during its transition period.* Played a key role in formulating initiatives that ensured operational stability and business continuity during the management transition, directly contributing to the achievement of critical corporate objectives.* Played a key role in managing company operations during the interim management period, driving cost reduction and enhancing employee engagement and management. Show less I directed and optimized key quality assurance processes, including validation procedures, work-in-process evaluations, internal audits, employee training, and GMP compliance, ensuring operational excellence and regulatory alignment within the quality operations department and the Manufacturing facility.I also partnered with the Research Manager to champion product development initiatives, oversee pilot-scale compounding, conduct stability studies and prepare product dossiers that supported successful regulatory approvals, and successful product launch of new products and line extensions contributing to the organization’s compliance and growth.• Spearheaded Neimeth's strategic engagement in the WHO Technical Assistance Programme for WHO prequalification, managing the comprehensive facility upgrade. • Forged and nurtured strategic partnerships with renowned research institutions, including NIPRD and BioResources, to accelerate the development and commercialization of phytomedicines. Show less

  • Member, Interim Executive Management

    Mar 2023 - Aug 2023

  • Quality Assurance and Assistant Research Manager

    Nov 2012 - Feb 2023
• 

  Neimeth international pharmaceuticals plc

  Mar 2013 - now

  Head, quality operations

  In my role as Head of Quality Operations, I have directed and streamlined all quality-related activities, including quality control & microbiological evaluation, GMP & GLP compliance, pharmaceutical quality assurance, validation and qualification, vendor audits, Product complaints, Regulatory and self-audits.My efforts have ensured regulatory adherence and operational excellence throughout the organization.I have successfully conducted and validated third-party audits of potential contract manufacturers in India, ensuring full compliance with international quality and operational standards. Additionally, I mobilized cross-functional teams for a multi-state drug supply project, guaranteeing the timely, accurate, and complaint-free delivery of critical pharmaceutical products.* Led and influenced strategic committees-including ethics & conduct, plant disciplinary, business development, intellectual property, canteen, and office aesthetics-delivering measurable outcomes via decisive leadership and effective collaboration.* Revamped quality operations by defining clear job roles and responsibilities, enhancing productivity, and elevating quality output-resulting in zero product recalls or product integrity issues throughout tenure.* Championed product introduction initiatives by leading formulation development, overseeing stability studies, and executing comprehensive dossier preparation for seamless regulatory approvals.* Pioneered transformative facility upgrades in manufacturing and quality operations, driving the factory's accreditation for NIS ISO 14001:2004 and facilitating a smooth transition to NIS ISO 9001:2015 certification. Show less