**Work mode**:Onsite**Onsite Location(s)**:Heredia, CR**Additional Locations**: N/A**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**
- At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer and has been recognized with the Catalyst Award in 2022, a prestigious recognition of diversity, equity and inclusion excellence. Also, we have a Gender Equality Policy to support our commitment.- Hybrid Roles:
- Boston Scientific's hybrid workplace includes WFH and onsite. You will have the opportunity to discuss details in the interview.**About the role**:
- Works cross-functionally to lead process development of complex technologies on new products and ensures efficient and effective transfer of new product into production.**You're Responsibilities include**:
- Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on platform or derivative projects.
- Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
- Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems.
- Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM's, Routers, FMEA's, etc.)
- Develops qualified production lines.
- May supervise Technicians and Eng I to achieve projects goals.
- Additional Duties:
- Oversees development builds associated with the project using special work requests.
- Writes and reviews validation protocols and reports applicable to new processes.
- Plans, organizes, and conducts all aspects of technical reviews.
- Provides Design for Manufacturability (DFM) input to the engineering print package.
- Contributes ideas to or generates Intellectual Property submissions.
- Trains and/or provides work direction to technicians and engineers and may train manufacturing personnel when required as part of a validation.
- May serve as a core team member or extended team member on new product projects.
**What We're Looking For**:
- Bachelor's degree in mechanical, Electromechanical, Electrical Engineering or equivalent
- English Level desired: B2+
- Experience: 5+ years
- Or an equivalent combination of education and experience.
- Desired knowledge: Process Validation, Problem Solving/ Process Improvement, Strong
- Technical Knowledge, Design for Manufacturability
- Proven technical knowledge, and Interest in developing as a strong, technical individual contributor.
**Requisition ID**:580563- **Benefits - Life-Work Integration - Community - Career Growth**
- At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination, and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life's work.**Job Segment**:Process Engineer, Manufacturing Engineer, Electrical Engineering, Engineer, Engineering, Quality