Process Engineer III

at  Boston Scientific Corporation

REQUIRED QUALIFICATIONS:

• BS in Mechanical Engineering or Biomedical Engineering (or related degree) with 5+ years of related working experience.
• Experience of fixturing development, automating systems and integrating equipment
• Demonstrated use of DOE and problem solving.
• Demonstrated ability to develop processes from concept to production.
• Demonstrated knowledge and application of Processes and Equipment validation techniques (IQ, OQ, PQ), process risk analysis and associated regulatory requirements.

PREFERRED QUALIFICATIONS:

• Demonstrated cross functional teamwork in technically demanding environment
• Demonstrated ability to develop and drive innovative solutions into processes and products.
• Expertise in New Product Development.
• Medical device or other regulated industry experience.
• Demonstrated understanding and usage of statistics to drive improvements.Open to travel of up to 10% of their time

ABOUT THE ROLE:

Boston Scientific is seeking a highly motivated and experienced engineer to work on process development for design and commercialization of new technologies across BSC. The candidate must have a desire to utilize their skills to solve technical/complex problems in a hands-on manner, working in a fast-paced environment, and across multiple functions in a global company. The successful candidate for this position will provide strong leadership and problem solving to enable medical device innovation. Use your technical and collaboration skills alongside your passion for innovation and continuous improvement to drive growth through efficient and effective commercialization of new products and targeted improvements. This position offers the opportunity to support process development and product commercialization throughout Boston’s global plant network. Works cross-functionally to develop capable process and complex technologies on new products and ensures efficient and effective transfer of product into production.

YOUR RESPONSIBILITIES WILL INCLUDE:

• Develops functional deliverables associated with the TDP/PDP, Project Management and Quality Systems. This includes Master Validation Plan, Process Risk Assessment, Validation Protocols, Reports, BOMs and Routers.
• Prepares and presents technical data and recommendations at technical reviews.
• Planning and execution of capital equipment acquisition
• Provides Design for Manufacturability (DFM) input.
• Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on multiple and moderately complex processes.
• Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
• Contributes ideas to or generates Intellectual Property submissions.