Quality Engineer - R&D, Medical Devices

We are seeking a skilled Quality Engineer. The ideal candidate will be responsible for implementing and maintaining our quality management system (QMS) throughout the product development lifecycle.
Key Responsibilities:
1.    Quality System Compliance: Ensure compliance with global regulatory requirements and standards for medical devices, including FDA QSR, ISO 13485, EU MDR, and others as applicable.
2.    Design Control & Risk Management: Participate in design control activities, ensuring quality considerations are integrated into product development processes. Lead risk management activities (FMEA, risk analysis) to identify and mitigate potential issues.
3.    Process Validation and Verification: Oversee the validation and verification of design and manufacturing processes. Ensure robust testing methodologies are applied to prove that designs meet all requirements and regulations.
4.    Documentation and Records: Write and Maintain comprehensive documentation that meets regulatory and company requirements throughout the product development lifecycle. Ensure traceability and accessibility of quality records.
5.    Cross-functional Collaboration: Work closely with R&D, manufacturing, regulatory affairs, and other departments to ensure quality is embedded in all aspects of product development and production.
6.    Training and Development: Provide quality engineering expertise and training to R&D and other teams. Stay updated on industry trends, regulatory changes, and best practices in quality management.