Abdullah AlDayel

Abdullah AlDayel

Trainee

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location of Abdullah AlDayelRiyadh, Riyadh, Saudi Arabia

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  • Timeline

  • About me

    Quality | Partnerships | Regulatory Affairs | Project Management Professional (PMP) | Governance, Risk, and Compliance (GRCP) | Certified Knowledge Manager (CKM) | Lean Six Sigma Black Belt (LSSBB) | Pharmacist

  • Education

    • King Saud University College of Business Administration

      2021 - 2022
      Master's degree Health and Hospital Administration
    • College of Pharmacy at King Saud University

      2008 - 2015
      Bachelor of Pharmacy (B.Pharm.) Pharmaceutical Sciences

      Activities and Societies: pharmacy students club, Hayat volunteer club

  • Experience

    • Health House Pharmacy

      Jul 2011 - Aug 2011
      Trainee

      community pharmacy training, including but not limited to: Pharmacy organization, patient interaction, PoS.

    • Kingdom Hospital & Consulting Clinics

      May 2014 - Jun 2014
      Trainee

      Hospital pharmacy training, including but not limited to: Prescription reviewing and preparation, dispensing, patient interaction and education, I.V. Mixing and preparation.

    • Medicine Umbrella

      Jan 2015 - May 2015
      Pharmacist

      Temporary job. Tasks included: receiving of medications, dispensing, patient education.

    • AJA Pharmaceutical Industries Co. Ltd.

      May 2015 - May 2018

      Created the department including all it's basic requirements.Responsible for products quality and patient safety. Processing and reporting and product defect, safety, and patient issues. Products review and approval.Factory and production line registrations and approvals with local authorities, including authority audits.Engaging and negotiating with local and international partners.Material reviews and approvals.Teams support.

      • Qualified Person Responsible for Pharmacovogilance

        Feb 2017 - May 2018
      • Regulatory Affairs Specialist

        May 2015 - May 2018
    • Medochemie Ltd

      May 2018 - Jul 2019

      Created the department including all it's basic requirements.Responsible for products quality and patient safety. Processing and reporting and product defect, safety, and patient issues. Creating the scientific office and all it's basic requirements.Fixing company issues and problems to be in accordance with local laws.Products review, and submissions.Material review and approval.Team support.Representing the company in front of local authorities.

      • Qualified Person Responsible for Pharmacovigilance

        May 2018 - Jul 2019
      • Regulatory Affairs Officer

        May 2018 - Jul 2019
    • Aspen Pharma Group

      Jul 2019 - Jul 2022
      Regulatory Affairs Associate

      Submission review and approval, material review and approval, team support, leading projects, updating the company and products in accordance with local laws, responding to authority issues and circulars, representing the company in front of the local authorities.

    • Amarox KSA

      Jan 2023 - Feb 2023
      Regulatory Affairs Specialist

      Supporting business operations for product registrations within the defined territoryProviding visibility and reporting of ongoing product registrations and its status and to other stakeholders with the use of the product registration trackers where requiredCommunication of expected product design changes received from Legal manufacturers onto distributors and authorities, collects such information from distributors and authorities on their impact and informs the Legal manufacturer and distributor on actions resulting from these changes.Communicating and clarifying when required, the registration requirements through to the Legal ManufacturersCommunicating and informing Sysmex legal manufacturers of relevant expected regulatory changes and keeping abreast of such changes in the defined territory.Providing updates to the management through regulatory intelligence gathered via Commercial team, Distributors and authorities in the designated territory.Working together with the Technical Service Team in collating information on any Potential Reportable Events in the designated territory.File Submission & direct interaction with SFDA; close follow up with the Authorities till registration is finalized.Shipments release: assessing the import/Export requirements for the products, reviewing and submitting required documents, and following up with competent authorities including SASO, MOC, MOI, and customs Show less

    • Authority of People with Disability APD هيئة رعاية الأشخاص ذوي الإعاقة

      Mar 2023 - now

      Manage tasks related to measuring and monitoring the organization's performance and issuing periodic reports.Take responsibility for consolidating and regularly updating the organization’s data on initiatives and indicators to serve as a unified source of information for all stakeholders.Oversee the integration and coordination with the team in analyzing strategic performance at the organizational level and issuing reports according to the approved timeline and governance standards.Lead efforts to analyze strategic objectives, study challenges, and identify opportunities for improvement while providing recommendations to enhance performance.Develop plans and propose methodologies to highlight the organization’s achievements and issue periodic reports showcasing these accomplishments.Maintain continuous coordination with supporting entities regarding performance and reports within the governance framework.Lead tasks related to assignments associated with managing the organization’s performance.Contribute to building internal team capabilities and empowering them to perform their duties efficiently.Analyze non-conformance cases within the department and take corrective actions.Set quality objectives and performance measurement indicators and monitor their progress to ensure stakeholder satisfaction.Prepare and oversee improvement projects and ensure their implementation to achieve organizational excellence. Show less Assist in identifying and researching potential partnership opportunities that align with organizational objectives and client needs.Support the preparation of partnership proposals and presentation materials that effectively communicate value propositions to potential partners.Collaborate with cross-functional teams to gather insights and develop partnership strategies that enhance overall organizational performance.Contribute to the monitoring and evaluation of ongoing partnerships to ensure alignment with goals and effective resource utilization.Engage with stakeholders to gather feedback on partnership initiatives and identify areas for improvement.Facilitate communication and information exchange among internal teams and external partners, ensuring transparency and collaboration.Participate in networking events and outreach initiatives to bolster partnership visibility and engagement within relevant sectors.Maintain detailed records of partnership interactions, negotiations, and outcomes to inform future partnership strategies.Support the design and implementation of partnership programs aimed at enhancing corporate relationship management.Conduct competitor analysis and market research to identify trends and potential impact on partnership opportunities.Assist in the development of reports highlighting the performance and impact of partnerships on organizational objectives.Take part in refining and optimizing partnership management processes to drive efficiency and effectiveness. Show less

      • Performance Specialist

        Mar 2024 - now
      • Partnerships Planning and Development Specialist

        Mar 2023 - Mar 2024
  • Licenses & Certifications

    • Training course in Photoshop

      King Saud University
      Oct 2012
    • Introduction to Drug Regulatory Affairs - SFDA & GCC Explained

      Bawazir Pharma Consulting Center
      Mar 2017
    • Pharmacovigilance Good Practices

      SFDA - هيئة الغذاء والدواء
      Apr 2017
    • SFDA Annual Conference

      SFDA - هيئة الغذاء والدواء
      Oct 2019
    • Introduction for Regulatory Affairs and SDR

      SFDA - هيئة الغذاء والدواء
      May 2016
    • SFDA Annual Conference

      SFDA - هيئة الغذاء والدواء
      Nov 2017
    • Mandatory Data and Documents For a Product Dossier

      SFDA - هيئة الغذاء والدواء
      Oct 2019
    • ECTD - E Submission Explained in GCC

      Bawazir Pharma Consulting Center
      Jan 2017
    • SFDA: Pharmacovigilance System Explained

      Bawazir Pharma Consulting Center
      Oct 2017
    • Training course in JAVA Programming

      King Saud University
      May 2012