Role Summary
This is an exciting opportunity to join our team as a Manufacturing Engineer and be part of the development of robust, capable, cost-effective & safe manufacturing processes. You will work closely with R&D and Manufacturing to support the transfer of new products & processes into commercial production.
About the Role
As a Manufacturing Engineer, you will be responsible for initiating and completing technical activities leading to new or improved products or process, preparing reports, publishing, and making presentations to communicate findings. You will research, develop, design, and evaluate mechanical and electro-mechanical processes and/or equipment, analyzing and solving problems from basic engineering principles, theories, and concepts through to complex and advanced problems.
Key Responsibilities:
* Initiate and complete technical activities leading to new or improved products or process, for next generation programs and to meet strategic goals and objectives of the company.
* Researches, develops, designs, and evaluates mechanical and electro-mechanical processes and/or equipment.
* Analyses and solves problems from basic engineering principles, theories, and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a breakthrough in technology.
* Demonstrates good working knowledge of DMAIC tools and applies these tools in the characterization, optimization, and troubleshooting of process equipment and technology performance.
* Introduces new processes, equipment, and materials including installation, calibration, EHS assessment, debug, and all associated process and quality system documentation requirements including technical and process work instructions.
* Demonstrates advanced technical expertise on process/product technologies to support design, optimisation, validation, and troubleshooting of those technologies, equipment, or materials.
* Demonstrates good working knowledge and application of Processes and equipment validation techniques (IQ, OQ, PQ), PFMEA's, and associated regulatory requirements and applies this knowledge in the support of efficient & timely validation of equipment and processes.
* Develops and supports more junior engineers in writing and release of process validation documentation including FMEA's, Validation Plans, protocols, and reports.
* Cultivates internal and external network of resources to complete tasks. May lead a project team, determining goals and objectives for the projects.
* Interacts cross-functionally and with internal and external customers. Serves as a consultant for engineering or scientific interpretations and advice on significant matters.
* Experience with catheter-based single-use devices is beneficial.
* Experience with electronic implantable devices is beneficial.
* Experience with CAD software and design skills are beneficial.
Requirements:
* Hons bachelors degree in relevant discipline
* Master's qualification in Engineering or Science discipline a distinct advantage
Boston Scientific maintains a prohibited substance free workplace.
Please be advised that certain US based positions require acceptable proof of COVID-19 vaccination status.