greenteg AG

Technology, Information and Internet

11-50

Full-time (permanent)

Switzerland

You always wanted to work in a young aspiring company? You have a profound knowledge in quality  
management and regulatory affairs in the industrial and medical field? You are  
motivated by new challenges and like to take a lead in solving them? You are a  
team player and a maker?

**Bingo! Then this is your chance.**

Your chance to become part of our greenTEG family.

## Tasks

*   Taking the lead in all quality related company affairs 
*   Developing and reviewing all quality requirements for management system documentation 
*   Guiding the company to ISO 13485 
*   Execution of internal and external audits 
*   Management of authority audits 
*   Continuous improvement of quality processes on product, production, and company level 
*   Certification (FDA and CEmed) of our medical products 
*   Introducing quality management software (eQMS) and concepts (LeanSixSigma) 
*   Teaching and controlling quality processes in the company

## Requirements

*   Completed studies in a technical field (physics, chemistry, material, or engineering  
    sciences) 
*   Profound knowledge in quality management / GMP / ISO 13485 
*   Several years of experience in quality management or regulatory affairs in the life  
    science or medical device field (FDA, CEmed) 
*   Preferably you have worked for an ISO 13485 certified medical device company, where you built up or improved the quality management system 
*   High quality awareness, persistence and distinct personal responsibility in project  
    management 
*   Strong analytic skills and a systematic problem-solving approach 
*   You have a good command of English (speaking, reading and writing) 
*   You work accurately, reliably and effectively 
*   You are a maker, an all-rounder and a team player

## Benefits

What we offer:  

An exciting quality management role in a fast growing med-tech company with own  
production facilities 

Possibility to take over responsibility for the further development of greenTEGs quality  
police and strategy on all levels (Company, Production, Product) 

Unique professional development opportunities  

Start-up mentality in a stable growth company 

A young, dynamic, international team

**What are you waiting for? Become a part of our greenTEG family.**

Bachelor degree completed

Employee

You always wanted to work in a young aspiring company? You have a profound knowledge in quality management and regulatory affairs in the industrial and medical field? You are motivated by new challenges and like to take a lead in solving them? You are a team player and a maker?
Bingo! Then this is your chance.
Your chance to become part of our greenTEG family.
<h2 id="tasks">Tasks</h2>
<ul>
<li>Taking the lead in all quality related company affairs </li>
<li>Developing and reviewing all quality requirements for management system documentation </li>
<li>Guiding the company to ISO 13485 </li>
<li>Execution of internal and external audits </li>
<li>Management of authority audits </li>
<li>Continuous improvement of quality processes on product, production, and company level </li>
<li>Certification (FDA and CEmed) of our medical products </li>
<li>Introducing quality management software (eQMS) and concepts (LeanSixSigma) </li>
<li>Teaching and controlling quality processes in the company</li>
</ul>
<h2 id="requirements">Requirements</h2>
<ul>
<li>Completed studies in a technical field (physics, chemistry, material, or engineering sciences) </li>
<li>Profound knowledge in quality management / GMP / ISO 13485 </li>
<li>Several years of experience in quality management or regulatory affairs in the life science or medical device field (FDA, CEmed) </li>
<li>Preferably you have worked for an ISO 13485 certified medical device company, where you built up or improved the quality management system </li>
<li>High quality awareness, persistence and distinct personal responsibility in project management </li>
<li>Strong analytic skills and a systematic problem-solving approach </li>
<li>You have a good command of English (speaking, reading and writing) </li>
<li>You work accurately, reliably and effectively </li>
<li>You are a maker, an all-rounder and a team player</li>
</ul>
<h2 id="benefits">Benefits</h2>
What we offer: 
An exciting quality management role in a fast growing med-tech company with own production facilities 
Possibility to take over responsibility for the further development of greenTEGs quality police and strategy on all levels (Company, Production, Product) 
Unique professional development opportunities 
Start-up mentality in a stable growth company 
A young, dynamic, international team
What are you waiting for? Become a part of our greenTEG family.

Quality Manager 80-100%

1 to 3 years

Data Scientist (m/w/d) 80-100%

Internship

R&D Internship: Researcher in Physiology (m/w/d) 100%

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