Nasıl hesaplanır?
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Son iş deneyimin, geçmiş deneyimlerin ve toplam deneyimin uygunluk puanını etkileyen kriterler arasındadır.
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Mesleki Yeterlilikler
Şirketlerin ilanda belirlediği kriterlerle özgeçmişindeki bilgilerin ne kadar uyumlu olduğu içerik karşılaştırılmasıyla bulunur.
Bu iş sana uygun olmayabilir

Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

Uygunluğunu nasıl hesapladık?
Diğer Bilgiler

QUALIFICATIONS AND JOB DESCRIPTION

QUALIFICATIONS

  • Graduated from universities' Science or Engineering Departments
  • Minimum 2 years Industrial / Process / Quality engineering or equivalent experience in manufacturing operations in international or national scale industrial companies
  • Quality management system standard experience (EN ISO9001, EN ISO13485)
  • Preferably, experience in the field of medical device quality management system and medical device regulation,
  • Experience in a regulated industry (Medical, Pharmaceutical, Consumer Product, Automotive, Aircraft, or Medical Device) is preferred.
  • Ability to audit production areas and identify non-compliance to requirements and develop/oversee action plans for corrective action is required
  • Excellent communication and teamwork skills
  • An organized, analytical approach to problem solving is also essential
  • Ability to adapt to change and deal with ambiguity
  • Full professional proficiency in English
  • Good knowledge of Ms Office applications
  • Completed military service for male candidates
  • Be able to reside in Ankara and Antalya

 

JOB DESCRIPTION

  • Supporting Production Director to manage the Plant Production -Quality Management System in compliance to relevant rules and policies, applicable standards and respective regulatory requirements.
  • To ensure production operation team is taking required actions for CAPA (Corrective And Preventing Actions) activities and also to support related teams & actors for production operation area
  • Manage the site Continuous Improvement Project Programs and maintain accurate project updates in the defined tracking system
  • Responsible for implementation of EN ISO 9001, EN ISO 13485 standards to current production process and practices, helping training organizations
  • Taking responsibility for production department corrective and preventive actions (CAPA) management process
  • Collaborate with partners across multiple functions, especially production operation, planning and Quality Control and Quality Assurance teams
  • Carry out preparation of statistics regarding quality of production and production KPI
  • Develop projects and manage special initiatives based on needs
  • Ensure that manufacturing operation is aligned
  • with production methodology and also has high quality standards for customer expectation perspective.
  • Taking active role for all other production related improvement projects and tasks

PREFERRED CANDIDATE

POSITION INFORMATION