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Research and Development Engineer

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Date: Jan 15, 2023

Location: Antalya, TR

Company: Getinge

 

 

At Getinge we have the passion to perform

 

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge, our passion is to secure that every person and community have access to the best possible care, offering hospitals and life science institutions products and solutions that aim to improve clinical results and optimize workflows. Every day we collaborate to make a true difference for our customers – and to save more lives.

Are you looking for an inspiring career? You just found it.

 

 

External Job Description Required.

Qualifications:

• 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)

• No military obligation for male canditates

• 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

Job Description:

• 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

Qualifications:

• 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)

• No military obligation for male canditates

• 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

Job Description:

• 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

 

About us 

Getinge is on an exciting transformation journey constantly looking for new ways to innovate together with our customers to meet the healthcare challenges of the future. We are committed to diversity, equity and inclusion and to sustainability with a goal to be CO2 neutral by 2025. We believe in giving our employees the flexibility they need and make every effort to foster a learning culture that supports their personal development and creativity. Our passionate people hold our brand promise ‘Passion for Life’ close to heart. 

 

If you share our passion and believe that saving lives is the greatest job in the world, then we look forward to receiving your application and resume. We hope you will join us on our journey to become the world’s most respected and trusted medtech company.