Staffing and Recruiting

gloor&lang AG

1-10

Switzerland

## Compliance to 14971 - life cycle management

Ready to work with a highly innovative and fast growing Medical Device Developer and Manufacturer with innovative services for global pharmaceutical companies? Be the new Teamlead to support the product development process of customized applications in terms of RISK Management.  

ISO 14971 emphasizes the need for a proactive and iterative approach to risk management, considering both known and foreseeable risks. Ongoing monitoring and evaluation of risks throughout the entire lifecycle of the medical device will be needed to thrive R&D forward. Compliance with ISO 14971 is a fundamental requirement, seeking regulatory approval for exciting new medical devices!  

You and your team are viable business partners in this critical product development process and keep track on various influencing factors during Design Transfer, Verification and Validation, Evaluation of Process and Product Risks with FMEA tools, usability testing till final Tech Transfer of the Processes on site till delivery to the customer.  

You are the interface between R&D, Industrialisation, Regulatory Affairs and customer stakeholders.  

__Your challenge:__  

* Team leadership and litigation: risk management
* Personnel, cost and resource management
* Structuring systematic RISK determination in the product life cycle
* Definition and coordination of measures in project and product management teams
* Creation, guidance and supervision of risk analyzes for medical devices according to 13'485 and 14'971

__Your profile:__  

* Degree in Mechatronics, Electronics, Software Engineering
* Experience life-cycle Management of highly innovative Medical Devices
* Knowledge of QA and Risk Assessment and relevant processes
* Experience with risk analysis and risk project management ISO 14'971
* Strong communication skills for liasing across departments and external customers
* Project Management and direct leadership experiences
* C1 English language skills, B1-B2 German skills would be an asset

Step into this highly visible role at the headquarters of an innovative Swiss manufacturer of modern devices. You will take over responsibility for planning and implementing the risk management process!

Employee

<h2 id="compliance-to-14971---life-cycle-management">Compliance to 14971 - life cycle management</h2>
Ready to work with a highly innovative and fast growing Medical Device Developer and Manufacturer with innovative services for global pharmaceutical companies? Be the new Teamlead to support the product development process of customized applications in terms of RISK Management. 
ISO 14971 emphasizes the need for a proactive and iterative approach to risk management, considering both known and foreseeable risks. Ongoing monitoring and evaluation of risks throughout the entire lifecycle of the medical device will be needed to thrive R&amp;D forward. Compliance with ISO 14971 is a fundamental requirement, seeking regulatory approval for exciting new medical devices! 
You and your team are viable business partners in this critical product development process and keep track on various influencing factors during Design Transfer, Verification and Validation, Evaluation of Process and Product Risks with FMEA tools, usability testing till final Tech Transfer of the Processes on site till delivery to the customer. 
You are the interface between R&amp;D, Industrialisation, Regulatory Affairs and customer stakeholders. 
Your challenge: 
<ul>
<li>Team leadership and litigation: risk management</li>
<li>Personnel, cost and resource management</li>
<li>Structuring systematic RISK determination in the product life cycle</li>
<li>Definition and coordination of measures in project and product management teams</li>
<li>Creation, guidance and supervision of risk analyzes for medical devices according to 13&#39;485 and 14&#39;971</li>
</ul>
Your profile: 
<ul>
<li>Degree in Mechatronics, Electronics, Software Engineering</li>
<li>Experience life-cycle Management of highly innovative Medical Devices</li>
<li>Knowledge of QA and Risk Assessment and relevant processes</li>
<li>Experience with risk analysis and risk project management ISO 14&#39;971</li>
<li>Strong communication skills for liasing across departments and external customers</li>
<li>Project Management and direct leadership experiences</li>
<li>C1 English language skills, B1-B2 German skills would be an asset</li>
</ul>
Step into this highly visible role at the headquarters of an innovative Swiss manufacturer of modern devices. You will take over responsibility for planning and implementing the risk management process!

Teamlead - Risk Management - Medical Devices

Apotheker:in mit Herstellungsfokus

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Engineer Pharma-Anlagenbau

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Apotheker:in mit Herstellungsfokus

Automation Software Engineer

Engineer Pharma-Anlagenbau

Fachspezialist*in Qualitätssicherung

Our other open positions
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