Stephen Ogedengbe Email & Phone Number

Canada

United Kingdom

Aseptic Technique: Execute aseptic procedures for the handling of sterile pharmaceutical materials and equipment to prevent contamination and maintain product integrity.Production Operations: Perform setup, operation, and cleaning of aseptic processing equipment including filling machines, isolators, and sterilization units according to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).Quality Control: Monitor production processes, equipment performance, and environmental conditions to ensure compliance with regulatory requirements and company standards. Perform routine inspections and document results accurately.Sterilization Procedures: Operate autoclaves, steam sterilizers, and other sterilization equipment to decontaminate materials and equipment used in aseptic processing.Documentation: Complete production documentation, batch records, and logbooks accurately and in a timely manner. Maintain comprehensive records of activities, deviations, and corrective actions.Safety: Adhere to safety protocols and guidelines to minimize risks associated with hazardous materials, equipment, and processes. Report any safety incidents or concerns promptly.Team Collaboration: Collaborate effectively with cross-functional teams including production, quality assurance, and maintenance to achieve production targets and resolve issues efficiently.Continuous Improvement: Participate in process improvement initiatives to optimize productivity, quality, and efficiency in aseptic operations. Identify areas for improvement and contribute ideas for enhancing processes and procedures.

United Kingdom

Collaborated with faculty members and research teams on ongoing research projects related to Biomedical Health. Assisted in designing experiments, collecting data, and analyzing results.Conducted literature reviews to stay updated with the latest developments in the field and contribute to the development of research proposals.Performed laboratory techniques such as cell culture, molecular biology assays, microscopy, and data analysis.Data Management: Collect, organize, and manage research data, ensuring accuracy and confidentiality.Publication Support: Assist in preparing research findings for publication in academic journals and presentations at conferences.Collaborated with faculty members in the preparation of course materials, assignments, and assessments for undergraduate and/or graduate courses in Biomedical Health.Attended classes and assist in conducting laboratory sessions, tutorials, and workshops and provided guidance and support to students during these activities Assisted in grading assignments, exams, and coursework. Provide constructive feedback to students.Attended departmental meetings, research group meetings, and seminars as required Served as a mentor to undergraduate students interested in research projects.

Nigeria

Provided clients with educational materials and information about the company's products and services to ensure customers were well-informed about the benefits of partnering with the company.Negotiated terms and contracts with clients, ensuring that agreements were mutually beneficial.Closed sales deals, securing long-term partnerships and contracts with retail businesses and hospitalsPrepared and delivered compelling sales presentations and proposals to potential clients whilst addressing the specific needs and challenges of each customer.Generated leads through various channels, including cold calling, networking, referrals, and digital marketing and prioritized them based on their potential value.Developed and implemented effective sales strategies to meet and exceed revenue and growth targets.Gathered feedback from customers and related them to internal stakeholders to identify areas for improvement.

Lagos

Assisted in the review and evaluation of drug applications and submissions to ensure compliance with FDA regulations which included analyzing clinical trial data, labeling, and product quality.Collaborated with staff to monitor the safety of marketed drugs. Assisted in adverse event reporting and signal detection activities.Prepared and maintained documentation related to drug approvals, regulatory actions, and compliance efforts. Participated in inspections and audits of pharmaceutical manufacturing facilities to assess compliance with FDA regulations. Assisted in preparing communication materials for healthcare professionals and the public regarding drug safety, recalls, and other relevant topics. Assisted in quality assurance activities related to drug products. which included reviewing batch records, stability data, and manufacturing practices.Education and Outreach: Participate in educational outreach activities, which may involve presenting information about FDA regulations and drug safety to healthcare professionals or the public.Policy Development: Contribute to the development of drug-related policies, guidelines, and regulations. Provide input based on your understanding of pharmacy practice and drug safety.Professional Development: Take advantage of learning opportunities and mentorship from experienced FDA staff. Attend training sessions, seminars, and workshops related to regulatory affairs and drug safety.Supported ongoing projects related to drug regulation, safety evaluation, and compliance initiatives. Assisted in project planning, data collection, and reporting.

Msc.Biomedical Health, Bioengineering And Biomedical Engineering

Master Of Business Administration - Mba, Marketing

Doctor Of Pharmacy - Pharmd, Pharmacy