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We care about people - Join the market leader



People every day all around the world will benefit from more personalized healthcare. The promise of better, faster, more cost efficient solutions is now within our grasp. And that’s the world in which Tecan plays a vital role – helping advance healthcare – through advanced life science research and diagnostic solutions. We constantly seek new ways to steer innovation.




Every lab. Every day. Empowered.



Our vision is to empower every laboratory, every day, around the world with Tecan technology, products and support. We will help to shape the future of automated workflows in life sciences and clinical diagnostics through unrivaled expertise, products and customer support.



We need you to join our Quality Management Team at our Head Office in Männedorf as

Quality Systems Specialist

What you will do

Reporting directly to the Head of Quality, the Quality Systems Specialist participates in all aspects of establishing, implementing, and maintaining the Quality Management System at Tecan. The position coordinates with R&D, Quality Control, and Operations to ensure the Quality Management System is kept current and is efficiently and properly maintained. As such, the individual must be familiar with ISO 13485/ISO 9001 and QSR. The individual must be able to prioritize activities associated with timelines and risk management from a quality perspective. 

Responsibilities will include

• Work in a fast-paced environment, assessing and managing dynamic priorities


• Work cross functionally across Quality with key department heads such as R&D/Operations and Service


• Actively assist in creating, implementing, and maintaining the QMS at Tecan, including writing the applicable SOPs, identifying required metrics for various programs


• Monitor QMS metrics, identify issues/root causes and develop any required resolution plans

What you bring along 

• Bachelor’s degree in a scientific or health-related field required


• Minimum of 3+ years of Quality Assurance experience in regulated life science environment


• Solid foundational understanding of cGMP principals in medical device manufacturing


• Ability to interact effectively with all levels of personnel within the organization


• Ability to serve on multiple interdepartmental teams and to act as team leader when appropriate


• Demonstrate strong organizational and interpersonal skills, building relationships with effective communication, influencing, conflict resolution, critical thinking, and problem solving with a keen attention to detail.


• Strong aptitude with Microsoft Office products (Word, Excel, etc.)


• Can confidently operate with ERP systems (SAP) and in house programs


• Fluent in German and English
  
  

What you will get

• Comprehensive Compensation and Benefits package


• Progressive employment conditions


• Exciting career opportunities


• Wide range of training courses


• Extremely attractive location overlooking the lake of Zurich


• International and diverse environment (30+ different nationalities)


• Strong company culture with rich history


• Global mindset with “Swissness” at heart

Do you want to make a significant difference in how the world is looking tomorrow and contribute to the innovation of state-of-the-art, cutting-edge technology products?

 

Look no further and apply now!

We are looking forward to receiving your application online. 

 

Applications from recruiters are welcome. Please register using this link: www.tecan.com/recruiters

 

Tecan Trading AG, Seestrasse 103, 8708 Männedorf, www.tecan.com

Location: Männedorf, Switzerland

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