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Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

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Son iş deneyimin, geçmiş deneyimlerin ve toplam deneyimin uygunluk puanını etkileyen kriterler arasındadır.
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Seçili özgeçmişindeki bilgilerle bu ilanın kriterlerleri sadece %30 uyumlu.

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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

GENEL NİTELİKLER VE İŞ TANIMI

Qualifications:

  • Minimum 5 years experience in QA (preferably within the Pharmaceutical Industry).
  • Proven track record in QA Management (inc. all relevant elements and processes of a suitable QMS) in a GMP/GDP/GCP/GxP environment.
  • Fully conversant with GMP/GDP (EU/TURKEY) and ISO 9001 requirements.
  • Accredited/Trained auditor of Quality Management Systems.
  • Member of Professional bodies related to Quality or the pharmaceutical industry (IRCA, CQI, RPS, RSC,AEFI etc.)
  • Experience with hosting regulatory (i.e. FAMHP, CBG/MEB,FDA) and clients audits.
  • Experience with creatiion, review and approval of Quality/Technical Agreements
  • Experience in developing and managing a QMS in compliance with GxP (GMP, GDP, GCp)
  • Excellent organisational skills
  • Good analytical skills
  • Excellent interpersonal, leadership, motivation and planning skills
  • Excellent communication skills (verbal & written) and diplomacy.
  • Team management experience
  • Computer literate (minimum intermediate level on use of MS Office element
  • Strong Managerial Skills
  • Ability to think proactively, positively and support business growth.
  • Commercial and business acumen


Job Describtion:

  • Compliance First - Prioritise full compliance with GMP, GDP, GCP, ISO 9001 and similar standards as well as DHL's GxP (Yellow Book) requirements to ensure Patient Safety – SISPQ (Safety, Integrity, Strength, Purity & Quality).
  • Development, management and maintenance of all required elements of the Quality Management System (QMS) to ensure compliance with Regulatory requirements, company’s internal quality policies and meet customer expectations.
  • Act as the "Responsible Person" or equivalent (i.e. QC Person) in their site and/or business units and be named as such in the relevant licences from the local authorities (or deputise accordingly within their team).
  • Lead digitalization of quality management processes and documentation
  • Perform internal audits on the quality system and reporting findings with request for corrective actions
  • Key Stakeholder in supporting the TURKEY senior management team with the delivery of the Quality and regulatory agenda and strategy at a regional/country/site/business unit level.
  • Attend customer MBR and QBR meetings, review service quality and develop action plans with operations.
  • Follow quarterly customer satisfaction surveys, record feedbacks, define action plans for improvement with all stakeholders and ensure correcive and preventive actions are in place.
  • Follow legislations to adopt company procedures and quality processes informing related stakeholders.
  • Ensure the evaluation of suppliers and requesting improvement from the suppliers with problems, Internal and external correspondence for complaints from customers
  • Determine validation and calibration needs of the equipments, systems in the company, make the calibration and keep records.
  • Provide quality trainings to company employees within the framework of Quality Management System,


Aday Kriterleri

Pozisyon Bilgileri