Process Development Engineer II

Purpose Statement:

Under supervisory direction, works closely with R&D and Manufacturing in the development of robust, capable, cost effective & safe manufacturing processes. equipment, materials and products and supports efficient and effective transfer of new products & processes into commercial production.

Job Responsibilities:

• Demonstrates basic technical expertise on process/product technologies to support design, optimisation, validation and troubleshooting of those technologies.

• Under supervisory direction, provides input to Equipment engineering or external equipment/tooling or material vendors in the selection, design & development of new (or upgrades to existing) equipment, tooling and materials.

• Demonstrates good working knowledge of DFSS/DMAIC tools and, with mentor assistance, applies these tools in the characterization, optimization and troubleshooting of process equipment and technology performance.

• Supports the development and execution of experimentation and testing to enable characterization, optimization and troubleshooting of processes and equipment.  and summarizes, analyses and draws conclusions from test results leading to effective technical resolution.

• Supports the introduction of 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.

• With mentor assistance demonstrates good working knowledge and application of Lean methodologies, and process improvement tools to assist in identification and elimination of "waste" process steps  and development of efficient, cost effective equipment and processes.

• With mentor assistance demonstrates good working knowledge and application of Process and equipment validation techniques, PFMEA’s, and associated regulatory requirements and applies this knowledge in the support of efficient & timely validation of equipment and processes.

• Under supervision supports the writing and release of process validation documentation including FMEA's, Validation Plans, protocols and reports.

Job Requirements:

• Bachelor's Degree in any Engineering discipline.
• Minimum 2-5 years of relevant experience in a manufacturing environment.
• Experience leading or supporting process improvement, quality improvement, or cost reduction projects.
• Professional certifications such as Lean Six Sigma, Quality, Validation, Project Management, or related certifications are an added advantage.
• Experience supporting New Product Introduction (NPI), product transfers, process validation, or equipment qualifications is an added advantage.
• Experience with vision inspection systems, automated inspection equipment, or machine vision technologies will be an added advantage.
• Strong analytical, problem-solving, communication, and teamwork skills.
• Ability to work effectively in a cross-functional environment and manage multiple priorities.
• Experience in the medical device industry is preferred.

About Us
As a global medical technology leader for more than 40 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.