r&d engineer

yayınlanma
şimdi başvur

iş ilanı detay

yayınlanma
lokasyon
antalya
sektör
Mühendislik
referans numarası
6464

iş tanımı

We are looking for a "R&D Engineer" for our multinational customer : Maquet Getinge who operates in the medical sector.

Management and handling of product documentation.
Proactive in finding permanent solutions for engineering&design problems.
Leads and / or supports the design, development and implementation of disposable devices and components.
Conduct design verification validation activities. ( shelf life, product performance testing etc.)
Creates, reviews and maintains technical documentation (DHF/DMR) according to established product development procedures and relevant regulations. (MDR / 21CFR820)
Closely collaborates with internal departments (Quality, Regulatory, Product Management, and Production) and external parties such as test laboratories, service providers and suppliers.
Evaluates and implements requirements from applicable standards.
Design management of new transfer projects including workflows, equipment, material, etc.
Taking an active role in the selection purchasing of equipments machinery.
Drive the integration of new technologies in terms of equipment designs/upgrades.
Developing implementing plans to improve quality, efficiency the reducing of costs.
Preparing the main database (BOP, BOM, equipment data, etc.) as well as monitoring revisions, applying the analyses to the Document Management System.
Management of internal improvement activities CAPAs.
Management and performing Process Product Validations Test Method Validations.
Actively contributing to engineering change control system.

nitelikler

Bachelor’s degree in Engineering; preferably Industrial / Mechanical/Material Engineering, Biomedical Engineering.
Preferably 3 years in an industrial environment and medical device development. (multinational company experience / medical industry is an asset)
Excellent command of both written spoken English; German is an asset.
Background and experience in project and production engineering.
Good knowledge of MS Office applications and an applicable knowledge of CAD. (AutoCAD,Solidworks)
Knowledge of statistical techniques.
Knowledge/experience of/with ISO 13485.
Knowledge /experienced of/in mechanical material testing (ISO/ASTM) and test method development.
Experience with medical device design control principals, Requirement Engineering and Risk management in Medical devices.
Good knowledge of problem solving tools. (knowledge of 6 Sigma tools is a plus)
Having ambition to develop his/her carreer in the medical industry.
Strongly creative with an analytical mind, able to use initiatives.
Able to work with multinational teams.
Good team working skills with the willingness to accomplish tasks in harmony with the other team members.
Interested and eager to learn update his/her knowledge.
Disciplined way of working with a high ability to concentrate on both processes results.
A critical mind with the desire ability to put designed solutions into practice.
Demonstrative experience in documenting work procedures.
Not restricted to work during night shifts.
Experience in Quality System Environment is an asset.
İşbu iş ilanına başvurmadan önce KVKK Aydınlatma Metni linkinde bulunan “aydınlatma beyanını” okumanız gerekmektedir. İşbu iş ilanına başvurmanız durumunda bahsedilen aydınlatma beyanını okuduğunuz ve kabul ettiğiniz addedilecektir.