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Product development engineer

Product development engineer

Randstad Professionals is currently looking for a Product development Engineer who will be assigned an interesting challenge for a major client based in Solothurn. 

This contract is an unique opportunity to join a major client, global group focusing on the Healthcare sector  (Medical device, Pharma/vaccines, Consumer health).

The initial assignment will start immediately and will last until 2019

                  

 

 

We are looking for an Engineer to accelerate new projects at our client's Resaerch & Development team. Primary focus will be on documentation production, Risk Management tasks (DFMEA/PFMEA), functional design requirements' Input/Output, verification and validations metrics. ENGLISH MANDATORY, GERMAN A PLUS.

Position duties and responsibilities:

- Designs and develops new implants and instruments and develops improvements and  modifications to current products according to the product development process

- Responsible for the product design

- Primary contact person for technical questions/issues of existing products

- Participates or leads product development projects

- Works with surgeons, sales force and others for design requirements, design concept development, prototype and cadaver evaluation, and clinical follow-up

- Responsible for initial patent review of designs for freedom to operate as well as for the protection of new concepts, techniques and products through proper patenting

- In close collaboration with the technical engineering office, generates product models, concept layouts, and prints using a CAD software

- Responsible for the performance of the product and its mechanical stability, as well as the application of geometric dimensioning and tolerancing

- Develops mechanical test set-ups (including derivation of benchmarks) according to national and international standards and coordinates the activities required to fabricate test parts and complete mechanical testing (according to PD process)

- Works with manufacturing during the design stages to incorporate manufacturability into the product designs and during the implementation phase to clarify design issues

- Performs the required activities and generates the appropriate PD documents to ensure compliance with national and international regulations related to medical devices (in particular EU MDD, US FDA, Japanese PAL)

- Supports surgeons with regards to handling of implants/instruments and engineering-specific questions

- Know and follow all laws and policies that apply to the job, and to maintain the highest levels of professionalism, ethics and compliance at all times

 

Education Requirements:

- University or ETH course plus 1-2 years practical experience or doctorate, or

- Experienced professional, who has mastered the job through professional training and extensive experience (min. 5 years)

- Knowledge of bio-mechanic, biology, anatomy is a plus

- Spread sheet and CAD/CAM, materials science

- Project management

 

Experience:

- Mechanical experience (construction, production), min. 1,5 - 2 years as Associate Development Engineer

Interpersonal skills / characteristics:

- Creative/problem-solving skills

- planning skills

- willingness to accept responsibility

 

For more information and your application, please contact:    

Olivier Worch
Consultant Life Sciences

Randstad Professionals (Schweiz) AG
Küchengasse 9
4051 Basel
T +41 58 201 55 55

olivier.worch@ch.randstad.com  

 

Gesamtbewertung

3,5

Basierend auf 18 Bewertungen

2,5 Karriere / Weiterbildung
2,5 Gehalt / Sozialleistungen
3,0 Work-Life-Balance
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