Delta Kozmetik San. ve Tic. Quality Assurance Manager İş İlanı

İşveren Hakkında
  • İstanbul(Asya)
  • Kozmetik, Hızlı Tüketim Malları
 İş İlanları

GENEL NİTELİKLER

Our company DELTA BRANDS, which was established in 1953, manufactures personal care, baby products and cleaning products in its own production facilities of 28.000 m2 in Istanbul Industry and Trade Free Zone / Tuzla.

We are looking for a Quality Assurance Manager to be assigned to our company's Quality Department.

QUALIFICATIONS AND REQUIREMENTS

  • Bachelor degree in Chemistry, Chemical Engineering or in similar field,
  • At least 7 years of Quality Management System experince,
  • Strong knowledge of FDA, ISO 9001:2015 and ANSI Standarts (455-3/455-4),
  • Have experince in cosmetics GMP (ISO 22716) and CFR 21,
  • Fluent in English both verbal and written and able to use his/her English to follow foreign literature,
  • Have the technical knowledge to defend the Quality Management System in audits,
  • Proficiency in MS Office programs,
  • Researcher, team player, strong communicatior and dynamic,
  • Leadership skills, to manage cross-functional projects and teams.
  • Math skills – data reporting, measuring, calibrating, and calculating specifications,
  • Critical thinking skills to help work through customer problems and production issues, as well as develop strategies for improving product quality.
  • Able to read blueprints, technical documents, and manuals,
  • Have strong desire to achieve the best and ensure top-quality products,
  • He/She must has an eye for detail to catch defects.


Şirketimizin Servis Güzergahları:

Tuzla - Uzunçayır arası (E5 üzerinden)

Tuzla - Aydınlı - Pendik - Kartal sahil

Tuzla- Esenyalı - Üst Kaynarca

Tuzla - Gebze - Darıca

Not: Belirtilen güzergâhlara uygun olmayan adayların başvuru yapmamaları önemle rica olunur.


JOB DESCRIPTION

  • To ensure develop and safequard quality standarts are carried out quickly and effectively,
  • Regularly auditing the production facility on ISO standards (ISO 9001, ISO 22716 cGMP), CFR 21 and ANSI standarts (455-3/455-4),
  • To ensure the establishment, implementation and initiation of necessary activities to prevent any nonconformity related to the Product, Process and Quality System,
  • To make risk analyzes related to the product and the facility, to determine the necessary actions to close the risks and to carry out activities to ensure that they are closed,
  • Preparing the necessary Quality documents requested by FDA or customers,
  • Working closely with the Senior Management to identify the company's deficiencies in terms of Quality Systems, to inform the management for the necessary investments, to produce solutions,
  • Establishing strategies to improve efficiency and profitability in the organization, as well as put out higher quality goods,
  • Conducting in-house audits of product inventory and documentation
  • To contribute to the development of the company in cooperation with all departments,
  • Testing and sampling products, ensuring they meet set standards and specifications,
  • Confirming all products are properly labeled before output,
  • Investigating customer complaints,
  • Assessing operational data and identifying quality problems.

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