Hakan Büyüker

Üretim Sorumlusu at gülsha
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Contact Information
Location
Istanbul, Istanbul, Turkey, TR

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Experience

    • Türkiye
    • Cosmetics
    • 1 - 100 Employee
    • Üretim Sorumlusu
      • Oct 2022 - Present
    • Türkiye
    • Biotechnology Research
    • 100 - 200 Employee
    • Auditor
      • Oct 2019 - Oct 2022

      To carry out audits on quality, product safety, GMP, hygiene, environmental management and occupational health / safety according to internationally accepted standards in food packaging, cosmetic, detergent and food supply chain manufacturing companies. To carry out audit programs as planned and communicated. To follow the current legislation related to the product categories and products inspected. Organizing / planning transportation for planned inspections. To prepare reports after the audits in accordance with the contracts and demands of the customers and submit them to the project manager for control. To closely monitor customer expectations and current audit demands, to ensure communication between the planning team and the audit team, to coordinate the audit practices. To follow the updates of the sources that make up the audit instructions and apply these updates to the instructions and audit methods. Ensuring that the necessary inspection equipment is supplied on time from relevant persons and resources. Ensuring the up-to-date calibrations of measurement equipment, performing periodic device accuracy tests and keeping traceable records. To ensure the initiation and follow-up of corrective and preventive activities by evaluating customer complaints and internal nonconformities. To work in accordance with the quality management system, to follow the revisions and to ensure the continuity of the system. To receive the quality management system documents, to deliver the old ones, to ensure that the documents are forwarded to the department personnel. Advising for non-food services. Providing trainings for non-food services. Fulfilling the requirements of quality assurance processes. Regularly creating and checking the documents that need to be submitted to the competent authorities during the inspections. Following the licensing processes of biocidal and cosmetic products. Execution of design, legal statements and UTS registration processes. Show less

    • Türkiye
    • Manufacturing
    • 1 - 100 Employee
      • Jan 2017 - Oct 2019

      Establishment, follow-up and reporting of daily liquid production plansTo ensure that the semi-finished product is produced in accordance with the GMP guidelines and the production instructions for the liquor to be produced according to the specifications To be able to solve the problems that may occur in the products during production and to make production controls and lot controls To create solutions in order to carry out the tasks easily during routine operation and to reduce the cost Make reductions from stocks of finished work orders To control the raw material inputs and outputs of the depot of the raw material section and to regulate the MSDS of the raw materials in the depotMonthly - annual census reporting Ensure that the preventive maintenance and calibration procedures of the equipment are carried out by the relevant technical team on time To provide the organization and administration of production workers To provide necessary trainings to the production staff, to monitor compliance with the instructions Provide for the safety and well-being of production team, and other personnel Analyzes manpower requirement based on customer demands and product loads Show less

      • May 2014 - Jan 2017

      The production process of planning, monitoring and reporting.

    • Türkiye
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Production Intern
      • Aug 2012 - Sep 2012

      To be ready with the weighing process of pharmaceutical raw materials,routine control of all stages of production and the production lines operate in accordance with the GMP rules. To be ready with the weighing process of pharmaceutical raw materials,routine control of all stages of production and the production lines operate in accordance with the GMP rules.

    • Mechanical Or Industrial Engineering
    • 1 - 100 Employee
    • Laboratory Intern
      • Aug 2010 - Sep 2010

      Analysis of metabolites in human. Analysis of metabolites in human.

Education

  • Kocaeli Üniversitesi
    Faculty Of Science And Letters, Chemistry
    2008 - 2012
  • Süleyman Demirel Anadolu Lisesi
    Science, 3,98
    2002 - 2006

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