Process Engineer II
Delivering on the promise of medical innovation begins at Boston Scientific.
By delivering innovative products that help clinicians improve the lives of patients every single day, Boston Scientific makes a profound impact on the quality of medical care around the world. As we continue to transform the field of medical technology, we seek dedicated individuals who possess the integrity and creative spirit needed to thrive in an innovative company. Join a global organization that is fueled by the diversity and talent of its entire workforce.
Process Engineer II - Medical Devices
Job Description:
Develop capable processes and ensure efficient and effective transfer of medical device products into production.
Key Responsibilities
Assess process capabilities, prioritize process improvement opportunities, and innovate and implement process improvements on multiple and moderately complex processes.
Apply Six Sigma tools, including DOE and statistical techniques, and technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
Execute the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems.
Prepare and present technical data and recommendations at technical reviews.
Write protocols, execute and write reports for process validation and verification (OQ/PQ/ATMV).
Ensure proper documentation is completed to meet quality systems requirements. (e.g., BOM’s, Routers, FMEA’s, etc.)
Oversee development builds associated with the project using special work requests.
Develop qualified production lines.
Provide Design for Manufacturability (DFM) input to the engineering print package.
Contribute ideas or generate Intellectual Property submissions.
Train and/or provide work direction to technicians and may train manufacturing personnel when required as part of a validation.
May serve as core team member or extended team member on new product projects.
Quality System Requirements
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Job Experience:
Requirements:
Typical minimum education/years experience: BS in Engineering/Technical field; 3-5 years of direct related experience. Advanced (Master) degree may be substituted for applicable experience. Medical device experience highly preferred. Ability to work effectively with all cross-functional groups. Excellent communication skills.
Minimum Education Required: Bachelor
Years of Experience Required: 3-5 Years
Expected Travel Time: None