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The Design Quality Engineer ensures that all medical device design and development activities meet safety, performance, and regulatory standards. This role partners with cross-functional teams to support new product development and sustaining engineering projects, driving quality, compliance, and risk management throughout the design lifecycle
We are seeking a Design Quality Engineer to join a medical device/regulated‑industry team. In this role, you will help ensure that products meet safety, regulatory, and business requirements throughout the design lifecycle. You will work closely with cross‑functional teams on both new product development and sustaining projects of complex electromechanical systems (with software and disposables).
The Design Quality Engineer plays a critical role in ensuring product designs meet regulatory and internal standards throughout development. This position leads risk management and supports design verification, while also contributing to CAPA investigations and continuous improvement efforts.
The Manufacturing Process Engineer will play a key role in optimizing manufacturing processes and ensuring product quality within the healthcare industry. This position involves collaborating with cross-functional teams to drive continuous improvement and operational efficiency.
The Senior Quality Systems Engineer plays a key role in driving compliance and continuous improvement across the organization's quality management systems. This role leads the CAPA program, internal audits, and quality metrics, ensuring issues are resolved through structured problem-solving and cross-functional collaboration.
As a Senior Program Manager in the life science industry, you will oversee complex projects within the engineering and manufacturing department, ensuring their successful execution from initiation to completion. This role requires strong leadership and organizational skills to manage cross-functional teams.
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