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Medical Device Expert - Design Review
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Engineering, Design
Projektbeschreibung
A pioneering global Medical Devices company is looking to appoint a Medical Device Expert - Design Review. You will be be responsible for the verification of product quality requirements with regards to resistance to degradation.
Responsibilities:
* Review product designs and manufacturing specifications to define product families and respective worst case representatives.
* Coordinate required product testing at the internal lab and document and rationalize verification results for the product families.
* Collaborate with the product development, design quality and test lab teams as well as manufacturing engineering to facilitate timely results.
* Information exchange and collaboration between internal, local, external and foreign partners is essential.
* Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
Education/Experience:
* Team player with strong initiative.
* Degree in engineering or natural sciences and preferably have some practical experience in a regulated industry.
* Self-motivated, systematic problem-solver with excellent communication skills
* Ability to take responsibility on projects.
* Keen interest in the interrelations between medicine and technology and a strong desire to work in a global company.
* Ability to communicate in both spoken and written English is required.
* Communication skills in German are highly preferred.
Please send CVs or call.
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Responsibilities:
* Review product designs and manufacturing specifications to define product families and respective worst case representatives.
* Coordinate required product testing at the internal lab and document and rationalize verification results for the product families.
* Collaborate with the product development, design quality and test lab teams as well as manufacturing engineering to facilitate timely results.
* Information exchange and collaboration between internal, local, external and foreign partners is essential.
* Close cooperation with internal departments, domestic and international authorities as well as the conscientious preparation of the required documents ensures compliance with Medical Device Regulations (EU MDD, US FDA, JP PAL).
Education/Experience:
* Team player with strong initiative.
* Degree in engineering or natural sciences and preferably have some practical experience in a regulated industry.
* Self-motivated, systematic problem-solver with excellent communication skills
* Ability to take responsibility on projects.
* Keen interest in the interrelations between medicine and technology and a strong desire to work in a global company.
* Ability to communicate in both spoken and written English is required.
* Communication skills in German are highly preferred.
Please send CVs or call.
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik