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Quality Technician à Émirats arabes unis

Sr. Specialist - Quality Compliance

Sr. Specialist - Quality Compliance
Julphar
Ras el Khaïmah
AED 25 000 - 45 000
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Sr. Specialist - Quality Compliance

Julphar
Ras el Khaïmah
AED 25 000 - 45 000
Description du poste

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.

Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

Summary Of The Responsibilities/Job Summary

  • Provide input to management so that they can make informed decisions
  • Keep management informed of actual or potential risks
  • Identify areas of opportunity for improvement
  • Assess personnel training effectiveness
  • Ensure ongoing compliance and conformity to regulations and standards
  • Determine system and process effectiveness and highlight the efficiencies.
  • Owning the Auditing system in Julphar for the internal Audits and External Audits

Detail Of The Job Responsibilities/Key Result Areas

  • Responsible for developing the internal audit schedule and its execution for all facilities of julphar.
  • Carry on the Lead Auditor responsibilities.
    • Communication with the client, for the Audit Preparation
    • Provides audit team selection input if requested to do so.
    • Communicates audit plan and requirements to auditee.
    • Plans the audit and directs the audit team.
    • Conducts audit process meetings.
    • Performs the audit to collect evidence to verify conformance or nonconformance to the audit criteria.
    • Verifies the correction of previous nonconformities if directed to do so
    • Prepares audit report.
    • Manages the audit process and resolves conflicts of interest or other personnel issues.
    • Ensures reports and records are properly filed and safeguarded
    • Reports conflicts of interest to the QA compliance Manager
    • Responsible for follow-up audit responses and writing of audit requirements to be met by individual departments through the checklist.
    • Follow up to get a timely receipt of responses from all applicable vendors and CMOs.
    • Training for the Co Auditors and coaching
    • Responsible for scheduling and execution of the external audits of Vendors, Contract Organizations, investigator sites, and other external organizations employed.
    • Maintain the audit reports and distribution/circulation to the vendors and track the vendor’s CAPA responses for closure on due dates with supportive evidence
    • Monthly evaluation of internal and external audit reports closed-out and pending actions for KPI and Quality Council Information.
    • To Perform any other responsibility assigned by QA Compliance Manager.
    • Support the Quality Management System improvement using the Quality Tools.
    • Manage the audits on the EQMS systems (Trackwise/Veeva/AmpelLogic)

    Core Competency

    • Professional knowledge in Quality Management systems
    • Technical Background related to the GMP areas (Sterile/Non Steile /Bio-Tech) and Laboratory testing
    • Completed the Auditor Qualifcation program
    • Risk Based Approach
    • Self confidence and indpendnacy
    • Good Communication skills and presentation skills
    • Ethical and adheres to an organization code of conduct and complies with the
    • principles of auditing as listed in ISO 19011, section 4
    • Knowlgable about the Quality improvement tools
    • Strong understanding and practice of 'cost consciousness'
    • Good on Process compliance & implementation skill

    Qualification/Functional knowledge

    • Batchelor or master’s degree in science/ Pharmacy
    • Experience of minimum of 3-7 years in the pharmaceutical industry preferably in Quality Management systems, and proven experience in Audit
    • Extensive Knowledge in cGMP and regulatory guidelines
    • MS Office proficeient
    • Statistical analysis is performed

    We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar
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    * Le salaire de référence se base sur les salaires cibles des leaders du marché dans leurs secteurs correspondants. Il vise à servir de guide pour aider les membres Premium à évaluer les postes vacants et contribuer aux négociations salariales. Le salaire de référence n’est pas fourni directement par l’entreprise et peut pourrait être beaucoup plus élevé ou plus bas.

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