Our customer, an internationally leading pharmaceutical company with headquarters in Basel, is looking for a
Medical Device Technical Expert (SaMD)
Your key responsibilities include:
* Support the ISO 13485 certification of our client for SaMD (Software as a Medical Device)
* Plan and write technical documentation
* Prepare the QMS update and participate in the notified body audit
* Support the transfer of a commercial app
* Support the design and implementation of cross functional resource tools for apps which are currently in the development stage
Your background includes:
* University degree in a relevant subject
* Work experience in the pharmaceutical or medical device industry
* Experience in planning and writing technical documentation for Medical Devices
* ISO 13485 and QMS for Medical Devices
* Experience with Medical Device Design Control
* Ideally experience in the field of SaMD
Assignment start: ideally October 2017
Assignment duration: planned until May 2018
Are you looking for an interesting and cutting-edge project as of autumn 2017?
Then please do not hesitate to send your complete application documents (CV, testimonials, diplomas) to Nicole Blum at Kelly Scientific Resources Basel nicole.blum(at)kellyservices.ch or apply online.
We are looking forward to getting to know you and to presenting your background and motivation to our client.