PROCESS ENGINEER JOB DETAILS | BOSTON SCIENTIFIC

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.
This position is responsible for designing and developing new and improved manufacturing processes and ensuring efficient and effective product transfer into production within the medical disposable devices industry.
Improve existing processes and implement new processes in the production line.
Job Responsibilities.
Develop and implement new manufacturing processes for production.
Perform Design of Experiments for process definition and optimize equipment parameters for new and/or existing processes.
Create documentation to support new and improved manufacturing processes.
Write and perform process validations (IQ, OQ, PQ) and validate methods for inspection, verification, and process controls.
Interface directly with assemblers, production supervisors, leads, and engineers.
Assesses process capabilities, innovates, and implements process improvements on key projects.
Applies technical knowledge to innovate, design, and develop processes, procedures, tooling, and/or automation.
Executes the functional deliverables associated with the NPI, Design Control, CAPA, and all Quality Systems.
As needed; plan, organize, and participate in all aspects of technical reviews.
Collaborate to ensure proper documentation is completed to meet quality systems requirements.
(e.
., GOIs, BOM’s, Routers, FMEA’s, etc.).
Job Requirements.
Bachelor's degree in mechanical engineering / biomedical engineering or related Engineering degree.
At least 5 years of demonstrated process development/improvement activities  Strong documentation skills- mandatory Equipment validations and process characterization and validation experience.
Prefer candidate from a Medical Device or other regulated industry experience.
Experience in FMEA documentation.
Demonstrated ability to develop processes from concept to production.
Excellent interpersonal and communication skills with good leadership abilities.
Excellent analytical and problem-solving skills in production environment, root cause analysis.
Performing investigation on product failures and defects.
Requisition ID.
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life.
Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate.
Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE.
BSX) isn’t just business, it’s personal.
And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!