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Quality Manager / Quality Engineer

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Elemed is Europe’s leading MedTech technical recruiter. We serve within the Medical device, diagnostic and combination device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow.

At Elemed, we recruit exceptional people that solve regulatory and compliance problems, so patients can have access to safe, innovative and life-changing Medical Devices.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status

Quality Manager / Quality Engineer

Title: Quality Assurance Specialist 

Location: Greater Zurich Area

Contact: monia@elemed.eu

The Company

 Join the company’s headquarters, based in a great location within the Greater Zurich area. This is a varied and responsible position in an innovative company that opens up long-term perspectives. 

A fantastic new and exclusive role has come in, with the opportunity to develop your career and knowledge in Quality. You will work with experts willing to develop your skills.

 As you learn and develop your skills, you will be provided the perfect platform to develop strategy for the department according to your own ideas and expertise; thus allowing you to leave a legacy within a company at their exciting point of growth. 

 The company is developing novel devices on a global scale. 

There are strong opportunities in the future for interesting evolution. 

The Opportunity

In this position you will be responsible for ensuring quality in terms of function, safety and compliance with regulatory requirements in their development and manufacturing phase. 

Your responsibilities (non exhaustive list):

  • Implementation and support of validation activities internally and with external partners (measuring equipment, software, production machines and processes) 

  • Monitoring of the production processes

  • Quality Assurance and batch releases

  • Supervision and implementation of internal and external audits

  • Contribution towards the creation of an efficient quality management system

  • Cooperation with risk management and post market surveillance team

  • CAPA evaluation and processing

  • Supporting R&D department with the interpretation of regulatory requirements and, if necessary during product development

  • Responsible for regulatory content of product - related information

  • Supervision and coordination of internal and external stakeholders in regards to complaint handling

  • Ensuring all specified quality and documentation requirements

Your qualifications:

  • Scientific or technical studies or equivalent

  • Experience in quality management in the medical device sector

  • Business fluent in German and English

If you are interested in this exciting role, please send your application directly to monia@elemed.eu

Would you like to find out more about our open opportunities? Visit https://www.elemed.eu/vacancies/

Please note: Only candidates meeting the requirements set out in the role profile above, will be considered in the application process. 

Due to the high volume of applications we receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful. 


Ms Elena Kyriacou
Heinrichstrasse 267 ? 267a
8005 Zürich

Website http://www.elemed.eu/

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