Baden-Württemberg: REGULATORY AFFAIRS MANAGER (m/f/d) - Medical Device für Tübingen gesucht
		Arbeits- und Stellenangebot im Regiobizz Arbeitsmarkt
        
        
        
        Job Kategorie: Medizin/Pharma/Biotech Medizin/Pharma/Pflege
		
          
        
            
              
Stellenangebot Basisdaten
            
            
                
                  - Arbeitsort:
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                    DE                    72070                    Tübingen                    
                  
- Umkreis:
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                  	keine Angabe.                  
- Art der Arbeitsstelle:
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- Letze Aktualisierung:
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                  	25.10.20252025-10-25
                  
 
         
		
		
        
        
            
              
Stellenausschreibung: Baden-Württemberg: REGULATORY AFFAIRS MANAGER (m/f/d) - Medical Device
            
          
            	
                
                  - Arbeitgeber bzw.
 Arbeitsvermittler
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                    Triga Consulting GmbH & Co KG in Hamburg
                  
                  - Branche
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                  	Medizin/Pharma/Biotech
                  
              - Kategorie
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                  	Medizin/Pharma/Pflege
                  
- Stellenbeschreibung
- Einleitung Our client develops, manufactures and distributes
cutting-edge surgical technology worldwide. At its location close to
TÜBINGEN, we are currently recruiting for a: REGULATORY AFFAIRS
MANAGER (m/f/d) Homeoffice: 50% Details: permanent position – 35
hrs. per week – 35 vacation days per year Aufgaben Preparation and
updating of technical documentation for medical devices in compliance
with MDR 2017/745 Ensuring compliance with applicable regulatory
requirements Development of test plans, organization of testing
procedures, and definition of test characteristics and equipment
Creation of standard test reports to demonstrate compliance with
relevant norms Acting as the main contact for notified bodies during
technical documentation reviews and regulatory inquiries from
development and production teams Defining regulatory strategies for
the approval of medical devices Qualifikation A completed degree in
engineering or natural sciences Professional experience in Regulatory
Affairs for medical devices Knowledge in the areas of ISO 13485 and
MDR Excellent German (C1) and English language skills, both written
and spoken Strong coordination and organizational skills Benefits What
TRIGA Offers You: New career perspectives and comprehensive consulting
for your personal RA career Positions that match your skills,
knowledge, and goals Exclusive job opportunities with background
information about the company Optimization of your application
documents and intensive preparation for interviews Direct access to
decision-makers and negotiation of the best compensation package Noch
ein paar Worte zum Schluss YOUR CONTACT: Silvio Di Meglio Managing
Director at TRIGA Consulting GmbH & Co. KG 089-8091307-21
- Qualifikation
- Arbeitskräfte
- Verdienst: 
- n.a.
- Bewerbung an
- Triga Consulting GmbH & Co KG
 Am Strandkai 1
 De 20457 Hamburg
 
 
         
        
        
		
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