Job Description:
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned.
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements.
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle.
Reports to Manager, Regulatory Affairs
Qualification and skills:
knowledge and demonstrated proficiency in the field of Regulatory Affairs andmedical device
perfect English verbal and written skills necessary
very good German skills preferred
must be team-oriented
project management skills necessary to be successful
negotiation skills necessary to be successful
MED-EL is a fast pace and high-tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com. We look forward to receiving your application via e-mail to: jobs@medel.com.
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
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