Design & Development Engineer facilitating new product development and registration for Cook Medical in China. Ensuring compliance with quality standards and regulatory requirements.
Responsibilities
Execute design and development projects ensuring all engineering activities follow established processes, technical standards, regulatory requirements, and quality management systems
Track milestones, document design decisions, and ensure deliverables are completed on time and within scope
Adhere to international and local regulations/standards throughout the project lifecycle, ensuring all engineering activities align with Cook Medical's Quality Management System and local regulatory requirements
Apply engineering expertise to support product development and transfer from concept to commercial launch, ensuring projects progress on time and in compliance
Drive technological innovation and contribute to the company's intellectual property portfolio through invention disclosures and patent applications
Collaborate with Engineering, Manufacturing, Quality, Regulatory, Marketing, and external partners to integrate resources and achieve project objectives
Provide engineering support for the implementation and improvement of the local Quality Management System (QMS)
Prepare and maintain documentation related to product concepts, design drawings, manufacturing processes, etc., ensuring compliance with regulatory and corporate quality requirements
Maintain accurate and timely project records and reports to support internal audits and external submissions
Work effectively with global teams, communicating proactively to achieve cross-regional project goals
Strictly comply with safety policies and procedures to ensure a safe working environment
Develop and maintain a thorough understanding of Cook Medical policies, procedures, and systems
Stay informed of updates in medical device regulations, standards, and guidance documents to ensure ongoing compliance
Requirements
Bachelor’s degree required, preferably in Engineering, Science or a related field
Minimum 3 years relevant experience is desired, preferably within the medical device industry
Knowledge of relevant ISO, EU, FDA medical device standards regulations is required
Strong technical writing skills
Proficiency in engineering software CAD required
Excellent communication skills in both English and Chinese required
Good mechanical design and understanding of engineering fundamentals with medical device materials knowledge is desired
Ability to collaborate effectively with local and global teams
Detail-oriented with strong problem-solving and project management skills
Execution of projects in a timely effective manner
Knowledge of anatomy and physiology desired
Self-motivated learner with the ability to work collaboratively and drive execution across functions
Willingness and availability to travel on company business
Fluency in Artificial Intelligence (AI) and data concepts
Benefits
Comprehensive engineering support
Opportunity to enhance intellectual property portfolio
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