Purpose/Objective:

This role works as the technical lead, system design owner and R&D interface in projects, together with product team, quality team and operation team to deliver pathology imaging products into China and global market.  

Area of Responsibilities:

 Lead R&D technical team in prdocut development, design transfer and product lauch with high quality delivrables.  Deliver DHF according to product design and development process, such as system/module requirements, product architecture, low level design of moudles.   Be responsible for converting user requirements and scenarios to design requirements and technical solutions.  Be responsible for leading system level and module level design of digital pathology scanner products in project, together with mechanical, electrical, optical, software design team.  Lead the feasibility study and verficication of new product design in early phase to manage system technical risk.  Lead the design for reliability and system reliability verification solution, to deliver highly reliable products for customers.  Lead R&D work in product development and V&V to ensure the product ontime delivery with high quality.  Lead the technical risk management activities such as DFEMA, DFR, DFM in projects.  Lead system integration activities such as Alpha sample integration and testing. Resolve the issues found in integration.  Be responsible for design change process to complete design update and release in NPD/Sustaining projects.

Person Specification：

Skills / Competencies

 Expertise in at least one domain in eletronical design, optical design, automation system design, etc. Strong understanding and application of System Engineering principles, processes, and procedures. Deep understanding in requirement engineering, product development process, design transfer process in medical device projects.  Skill in system modeling language, such as UML.  Technical leadership in system planning/integration.  In-depth knowledge and experience about the medical device related regulations, such as ISO 13485, FDA Title 21 CFR Part 820, ISO 14971, IEC 61010-1 etc.  Good knowledge about IP and patent management.  Good team collaboration in cross function team.  Strong systematic thinking skill.  Highly self-motivated and commitment to on time delivery.  Act initiatively and proactively. Technical leadership and mentoring.  Good integrity.

Functional Knowledge

Demonstrates and applies conceptual and practical expertise in own discipline and is able to apply knowledge in related disciplines.

Business expertise

   Applies knowledge of best practices and analyzes which best practices should be applied in own team to achieve differientation in the market.

Leadership

  Acts as a resource for colleagues with less experience; may lead small projects with manageable risks and resource requirements

Problem solving

 Demonstrated ability to leverage PSP to solve complex  problems independently; takes a new  perspective on existing  solutions; exercises  judgment based on limited set of data.

Impact

   Impacts a range of customer, operational, project or service activities within own team and other related teams; works within broad guidelines and policies.

Interpersonal Skills

   Explains difficult or sensitive information; works to build consensus.

Education

Master’s degree or above in Engineering.

Experience

Minimum of eight (8) years of systems engineering and integration experience within medical device field.Successful experience in product design, design transfer and design change management in medical device projects.At least 2 successful complete product release experiences.

 Language

 Fluent English listening, speaking, and writing.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.