19 ott - Milano
Empatica
As a Quality Assurance Specialist at Empatica, you will be a key member of the Quality and Regulatory Department, supporting the maintenance of the Quality Management System as well as:
• Champion Quality culture and compliance within the different development teams, supporting them in the compliance effort
• Continually seeks to drive improvements in product and process quality
• Provides the quality/independent review at defined design reviews, design plans, risk management, design verification/validation protocols and reports, for new development projects as well as design/process changes to existing products
• Support team in performing required Risk Management activities
• Support Engineering manager with the activities related to change management and new product development. Support developers in creating design control documentation, making sure product requirements and regulatory requirements are aligned
• Support Design transfer activities to ensure quality compliance of the manufacturing process
• Interfaces with Regulatory Affairs, Clinical Science, Marketing,
and product manager to translate their needs in actionable and regulatory compliant requirements.
• Implement, maintain and update procedures that ensure that the design control process constantly meets Empatica's and regulatory requirements
• Support Regulatory affairs in drafting EU Technical Documentation and US 510(k)s and De Novo submissions
• Ensure production activities are compliant with internal procedures and internationally applicable standards
• Keeps up to date on all ISO/EN/FDA/MDR and other Product Development related regulatory requirements and relay this information to the Product Development group
Requirements
The ideal candidate for this role:
• Has a genuine interest, passion and motivation for Empatica's mission
• Has a strong academic background, BS or MS in Biomedical Engineering
• Has at least 3 years of experience as a Quality Assurance Specialist, Design Quality Engine
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