Validation Supervisor Biofarma İlaç

İstanbul(Avr.), İstanbul(Asya)

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

GENEL NİTELİKLER VE İŞ TANIMI

 

·         Graduated from Chemical, Chemical Engineering or Pharmacy departments of universities,

·         At least 5 years of experience in similar positions in the pharmaceutical sector,

  • Min. 2 years of work experience as a Executive, excellent people management qualities,

·         Has personally worked on Process Verification, Cleaning Verification and Computerized System Verification and has professional knowledge,

·         To have documentation experience in accordance with GMP,

·         Familiar with SAP, QMex, BMS systems,

·         Experienced in production and laboratory equipment software validation

·         Knowledge about GAMP5 and data integrity approach,

  • Training, leading and motivating validation team and cross functional teams,

·         Good use of MS Office programs,

·         Good command of English,

·         Result oriented and open to improvement,

·         Planning, reporting and analysis skills,

·         Strong analytical thinking and problem solving skills,

·         Taking initiative,

·         To have completed military service for male candidates,

 

JOB DESCRIPTION

·         To perform process, cleaning, computerized systems validation (CSV) studies for new systems to be established, to perform them within the time schedule specified in master plans, to make periodic reviews,

·         Taking validation actions at the point of releasing process validation batches,

·         Optimization of cleaning approach in-house, organization of quality improvement and cost reduction studies

·         Ensure that all process, cleaning, CSV documentation and approach within the company complies with the requirements,

·         Review, approve and arrange user authorizations in GMP-critical systems in terms of validation.

·         Conducting studies in the context of data integrity.

Aday Kriterleri

Pozisyon Bilgileri