Development Engineer

A top 10 pharmaceutical company is seeking a Development Engineer to join their offices in Oberdorf, Switzerland on a contract basis.

Job Responsibilities:

• Responsible for the design and development role for the independently update of the technical documentation of existing electromechanical medical devices according to MDR Responsibilities
• Update of technical documentation (e.g. Product Risk Management, Design Requirements, Design Outputs) according to MDR regulations and internal processes
• Performs the required activities (e.g. create rationales, decision finding protocols) and generates the appropriate PD documents to ensure compliance with national and international regulations related to medical devices (MDR, US FDA, Japanese PAL, ISO 13485)
• Works together with regulatory, quality, technical engineering, external suppliers and manufacturing to release the documents
• Knowledge and compliance with laws and policies that apply to the job and ensure a high level of professionalism, ethics and compliance at all time

Education, Skills and Experience:

• Master/bachelors degree in mechanical/mechatronics/electrical or design quality engineering
• At least 3 years of experience in the design and development of medical devices
• Business fluent in German and English
• MS Office (Work, Excel) knowledge is required.
• Creative/problem-solving skills

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Caleb Mensah on +44 203 854 1080 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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