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Bu iş sana uygun olmayabilir

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.
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

About NephroCan:

 

NephroCan INC. is a family owned Canadian company committed to improving the quality of life for patients with End Stage Renal Disease (ESRD). As a trusted partner in the field,  we strive to offer the A to Z of hemodialysis consumables and machinery.

For over a decade, we at NephroCan have been providing research and development for companies specializing in the dialysis industry, catering to patients globally. Consistently working to offer the highest quality hemodialysis products, our promise is to improve therapy methods year after year.

With our accumulated knowledge and over 25 years of expertise, NephroCan is comprised of nephrologists, medical doctors, nurses, engineers, quality management professionals, business leaders, and a vast research and development team. This allows us to provide reliable care to our dialysis patients and partners worldwide.

NephroCan Medikal Sanayi Ticaret A.S is a subsidiary of the Canadian company, NephroCan Inc., and is one of the production facilities around the world.

Key responsibilities:

  • Perform research and feasibility studies on the improvement of current products or production of prototype and new products.
  • Design and develop new products as well as lead product design verification and validation to satisfy product and customer requirements.
  • Ensure quality in a product’s design for usability, reliability, functionality, marketability, and manufacturability.
  • Responsible for investigating risk management for designing and developing products.
  • Responsible for updating the list of official standards used in all related processes.
  • Participate in obtaining manufacturing permits and legal permissions, preparation of technical files, OPC, and BOM for products.
  • Responsible for preparation of standards for parts and products, and other related documents.
  • Examine technical documents to verify the adequacy and accuracy of information, and ensure compliance with the standard and legal requirements.

 

Job qualifications:

  • University degree with a focus in Mechanical Engineering, Chemical Engineering, Polymer Engineering, Medical Engineering, or Pure Chemistry
  • Minimum 2 years experience in R & D field of medical or pharmaceutical industries.
  • Very good English level (interview will be conducted in English)
  • Strong familiarity with product’s design and development principals and processes
  • Familiarity with preparing technical files including CTD (Common Technical Document) and DMF (Drug Master File)

PREFERRED CANDIDATE

POSITION INFORMATION

Firma Sektörü:

Tıbbi Cihaz ve Malzemeler

Çalışma Şekli:

Haftaiçi 08.30 - 18.00

Sosyal / Yan Haklar:

Servis
Yemekhane

Çalışan Sayısı:

100-149