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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:
Your profile:
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!
Full Time