Requirements

Required education level
Bac. / Federal Vocational Bac., Ad. Federal PET / Fed. PET Diploma, Bachelor
Required experience
Between 1 and 3 years
Required language knowledge
English German
Required skills
English Medical Devices German MEDICAL DEVICES post market surveillance GERMAN medical devices german english Medical devices quality assurance ISO 13485 austria CAPA AUSTRIA Quality Assurance Austria German complaints vigilance class III hospital surgeon regulated industry ENGLISH Hospital Quality assurance Class III QUALITY ASSURANCE Vigilance Complaints

Details

Location
Other countries
Term of employment
Full time
Sector
Medical technology
Professions
CNC / Machine operator Design / CAD / CAM Quality Control / Processes Management / Project Managemen... Electronics / Electrotechnical Alternative / Renewable energy Environment / Safety Engineer / R & D Mechanic (Precision / Micro /... Car Mechanic / Car Electrician... Preparatory Work / Production Manual Worker / Qualified Manu... After-Sales Service / Maintena... Speciality of Watchmaking Technical-commercial Business- / Requirement Analys... Consulting / Management / Proj... SAP Project Management / Consu... Data Warehouse / Business Inte... Software Development / Softwar... Web Development / Publishing /... ERP (Oracle, Sage, Infor, Micr... Helpdesk / Support / Training Networks / Security / Hardware Database specialist / Architec... SAP Basis / Module Specialist System Technician / - Administ... Testing / Audit / Release Mana...

Description

Post market surveillance / Complaints specialist - Class III Med Dev products - Scenic Austria - strong commitment to training and development
Located amongst postcard perfect scenery in Austria, our client is a leader, developing and commercialising innovative electrical/micro-electronic medical device products internationally. A fabulous opportunity has just arisen to join as a Complaints investigator and post market surveillance specialist, performing incident reporting and other vigilance activities and coordination of recalls and field actions. Tasks would also include the monitoring of product performance, quality data trending and reliability analysis, review of complaints investigations including root cause identification, establishing and maintaining quality system related work flows, and generally ensuring all activities are compliant to local and international regulations (ISO 13485).

Fabulous young company with big plans and many opportunities to offer. English is the corporate language, and with German very beneficial. Free German lessons and relocation assistance are amongst the benefits that come with an attractive salary package.

For more information on this vacancy, please contact the Senior Consultant Andrew Boroky on 0041 43 50 80 816, and email him your resume in WORD format to quality@nonstop-devices.com.

Keywords: Returned Devices Adverse Events, Compliance, clinical, data management, post market surveillance, trending, manufacturing, R&D, Research and Development, Quality Management, complaints handling, technical, ISO 13485, FMEA, Medical devices, root cause analysis, QMS, CAPA, Austria, Nonstop Recruitment

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

NonStop Consulting
Not available

Contact info

NonStop Consulting
Andrew Boroky
10w yw y- z7 )y( 07g
Not available