Overview


Título del trabajo: Manufacturing Engineer Iii / Project Engineer Iii

Compañía: Boston Scientific

Descripción de funciones: **Work mode**:Onsite**Onsite Location(s)**:Cartago, 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**:- Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area.**Your Responsibilities Include**:- Works actively on projects to optimize the different processes, to achieve yield improvements, cycle time improvements, and scrap reduction.- Collaborates cross functionally to understand design inputs and outputs on acquired entity’s design control structure.- Performs documentation remediation including process risk management, validation plans, validation executions, test method validation executions, manufacturing instructions, training plans, and new process development to ensure requirements of the BSC quality system are achieved.- Define business requirements and the Standard Operating Procedures related to manufacturing processes driven by the Boston Scientific Quality System to support production and business goals.- Participates in project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments.- Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.- Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.- Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements.- Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor.- Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.- Acts independently to implement and follow through.- Perform root cause analysis of failed product.- Participates in project planning and scheduling.- Attends and contributes to product core team meetings.- Performs responsibilities required by the Quality System and other duties as assigned or requested.**What we’re looking for**:- Licenciature degree in Mechanical, Electromechanical, Electronic, Biomedical, Chemistry, Industrial, Electrical, Materials Industrial Maintenance.- English Level desired: 80-85%.- Experience: At least 3 years- Able to coordinate tasks with different functions to ensure execution of assigned deliverables.- Desired knowledge: «Process Manufacturing Certification», Problem Solving, Regulatory industry management, Regulatory Affair, Networking, Process Validations, Stadistical and Experimental Analysis, DOE, Solid Works, Transfer Process, MiniTab, Hands &Statisctics, Tools (Statistics, Technical Manuals, Kaizen, Six Sigma), Regulatory industry management.**Requisition ID**:579578- **Benefits – Life-Work Integration – Community – Career Growth**- At Boston Scientific, you will find a collabo

Ubicación: Cartago

Fecha del trabajo: Wed, 13 Mar 2024 23:49:49 GMT