Femi Awosedo Email & Phone Number

Lekki, La, Ng

Chemin De Blandonnet 8 Cp 401 1214 Vernier (Geneva) Switzerland

Development of ISO standardsInternational Workshop AgreementContributing and reviewing of ISO standards

Ikota,Ajah Lagos

Governance- Development of QHSE policy, manual and procedure.Ensures adherence to QHSE standards and processes.Review of organization documents to meet statutory and regulatory requirements.Monitors and evaluates quality metrics.Preparation of Annual Action Plan.Vendor management.Implements corrective actions as needed.Facilitates smooth transitions during organizational changes.Communicates changes to stakeholders.Compliance- Review of organisational procedures and processes in line with QHS manual/policy.Conducting Internal and spot audits to identify conformance/no conformance to the QHS policy. Implementation of the ISO 9001, 27001 and 45001, standards within the organisation.Manages the certification process (e.g., ISO certifications).Ensures ongoing compliance with certification requirements.Preparation and presentation of internal audit reports to Top Management.Preparation of Management Review.Facilitates external audits by regulatory bodies or certification agencies.Prepares necessary documentation and coordinates audit activities.Coordinate and implement organization CRAMRisk management- Identifying risks associated with the organization and QHS objectives.Identifies, assesses, and manages risks.Develops risk mitigation strategies.Identifies potential hazards in the workplace.Implements measures to prevent or mitigate risksConducts strategic analyses to assess organizational strengths, weaknesses, opportunities, threats, and external factors.Business Continuity:Develops and maintains the organization’s business continuity plan.Ensures alignment with industry best practices and standards.Conducts Business Impact Analysis to assess the impact of disruptions on critical business processes.Identifies recovery priorities and strategies.Establishes crisis management procedures.Coordinates responses during emergencies or crises.Develops contingency plans for various scenarios.Ensures effective response and recovery.

Vahrenwalder Straße 269A 30179 Hannover Germany

1555 Boul De L'Avenir, Bureau 306, Laval, Quebec H7S 2N5, Canada

Conduct audits on behalf of MSECB for ISO 9001:22015 and ISO 45001:2018

6683 Jean Talon E, Suite 336 Montreal, H1S 0A5, Qc, Canada

As a Certified Trainer of PECB-Canada, I'm authorized to deliver training on ISO 27002 ISMS, ISO 9001, ISO 21502, ISO 45001 Lead Auditor, ISO/IEC 27001:2022 Transition and help individuals to get certificates like Fd = Foundation,LI = Lead Implementer,XP = Experience,mgr = Manager,LA= Lead Auditor

Nigeria, Ibeju Lekki Lagos

 Draft quality assurance policies and procedures, standards and/or specifications Interpret and implement quality control standards. Evaluate adequacy of quality control standards Devise sampling procedures and directions for recording and reporting quality data. Review the implementation and efficiency of quality and inspection systems Plan, conduct and monitor testing and inspection of materials and products to ensure finished product quality. Assessing customer requirements and ensuring that these are met Directing objectives to maximise profitability Responsible for declaring that a product is not safe or is not of the specified quality. Document internal audits and other quality assurance activities Investigate customer complaints and non-conformance issues Collect and compile statistical quality data Analyze data to identify areas for improvement in the quality system Develop, recommend and monitor corrective and preventive actions Prepare reports to communicate outcomes of quality activities Supervise the Quality Control unit. Identify training needs and organize training interventions to meet quality standards Coordinate and support on-site audits conducted by Internal and external providers Evaluate audit findings and implement appropriate corrective actions Monitor risk management activities Responsible for document management systems Assure ongoing compliance with quality and industry regulatory requirements Comply with information security policy of the company

Sango Ota Ogun

IN-PROCESS CONTROL OFFICEREnsuring Compliances With cGMPs In Factory Operations Good House Keeping Quality Management System Document Development Documentation and Record keeping Packaging materials development Product development member Qualification and Validation committee member Writing and reviewing of SOPs Batch records evaluation Ensure proper status labels in all raw materials, finished products Packaging material in the warehouse  Proper record keeping of humidity and temperature in processing area In Process Control Of Manufacturing Process Online Testing Of Intermediary Parameters; Determination of moisture content of granules. In-process control packaging Physical parameters analysis of products Ensure proper labelling of each mixed material from mixing section Sampling of bulk and intermediary products for chemical/ microbiological analysis. Raw/ packaging materials Suppliers audit Sampling and analysis of packaging materials CAPA tracking Self-inspection

Aswani Lagos

 Ensuring Compliances With cGMPs In Factory Operations Good House Keeping BMR evaluation Documentation and Record keeping Writing and reviewing of SOPs Production line clearance Maintenance of retention sample Ensure proper status labels in all raw materials, finished products packaging material in the warehouse  Proper record keeping of humidity and temperature in processing area In Process Control Of Manufacturing Process Online Testing Of Intermediary Parameters Packaging material development Suppliers audit Sampling and analysis of packaging materials

Sango Ota

CHEMICAL SECTION Routine and non-routine chemical analysis of drugs product using standard operating procedure. Writing and executing chemical testing procedures. maintenance of up-to-date documents for chemical testing methods and activities Operate laboratory equipment safety and effectively to conduct testing Recording, analyzing and reporting of test results to the QC supervisor Maintenance of inventory of chemicals and supplies in laboratory Validation of analytical method Calibration of analytical equipment Stability study IN-PROCESS SECTION Packaging material development Suppliers audit Sampling and analysis of packaging materials Monitoring of various production process• Cream and ointment floor• Tablet, caplet and capsules production floor• Syrup, suspension and lotion production floor• Sterile production floor Sampling of blends products for chemical and microbiological analysis Physical parameters analysis on Tablets, Caplet and Capsules before compression Inspection and monitoring of weight variation of tablets and caplets during compression Environmental monitoring (Temperature and relative humidity) of manufacturing area and warehouses Inspection and audit of raw materials in Pharmacy In-process file sample inspection and maintenance Determination of penetrating value of cream, ointment and gel products Leakage test on blister and stripped products General DocumentationMICROBIOLOGY SECTION Water analysis Line clearance Analysis of raw material Bio-assay Micro-organisms identification test Product microbial limit test

Pgd, Drug Development

Activities and Societies: Drug Developer University of Ibadan Faculty: Pharmacy Depart: CDDDP

Hnd, Microbiology, General, Distinction

National Diploma, Science Laboratory Technology, Upper Credit