Job Description
Additional Location(s): N/A
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information, and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing – whatever your ambitions.
Purpose Statement:
Under minimum supervision or direction, works closely with R&D and Manufacturing in the development of robust, capable, cost-effective & safe manufacturing processes to support the transfer of new products & processes into commercial production.
Key Responsibilities:
- Initiates and completes technical activities leading to new or improved products or processes for next-generation programs and to meet strategic goals and objectives of the company.
- Prepares reports, publishes, and makes presentations to communicate findings.
- 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.
Qualifications:
Hons bachelor's degree in relevant discipline. Master's qualification in Engineering or Science discipline a distinct advantage.
Requisition ID: 585817
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