At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job Overview
Functional Job Family Description
This position will provide engineering support to production through improvement or implementation of methods, processes, fixtures and tools. Additionally, you will propose and/or execute electro-mechanical improvements that result in improved cycle times. Position Responsibilities include, but are not limited to, validation, maintenance and introduction of new equipment and processes, including supporting documentation within an ISO 13485 environment. Develop training tools that facilitate compliance with TE Connectivity Standard Operating Procedures (SOP).
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KEY RESPONSIBILITIES& TASKS
Responsibility Includes the Following Tasks
- Learn, apply and share knowledge of products, manufacturing processes and equipment.
- Lead or participate in projects to maximize productivity.
- Lead or participate in cost reduction projects, such as: scrap reduction, flow improvement, inventory reduction, cycle time reduction, etc.
- Monitor manufacturing process activities, measure important process characteristics and analyze variation in order to detect and reduce waste.
- Analyze and provide information for decision making related to the outcome of key indicators for the manufacturing process.
- Lead or participate in the introduction of new part numbers into an existing technology platform or process.
- Lead process and equipment validations (IQ, OQ, PQ).
- Sourcing and implementing new technologies that maximize the operation. E.g. Obsolescence, increased capacity, versatility, ergonomics, etc.
- Participate in the activities of multidisciplinary teams for the solution of problems related to product quality (NCMR's, CARS, SCARS, CAPA's, etc.)
- All other functions with respect to the manufacturing process.
What your background should look like:
COMPETENCIES & SKILLS
• Ethics and Values- Commitment with quality and effectiveness.
Skills- Completion of improvement projects according to the defined date.
Abilities
• Ability to Work under pressure.
• Ease of adapting to change.
• Closing of CAPA's, NCMR's on the assigned date.
• Search for continuous improvement.
• Validation Compliance.
EXPERIENCE & EDUCATIONAL REQUIREMENTS
Experience
• Desirable 2 years of experience in medical industry process development, process/equipment validation or production line support.
• Knowledge of FDA and/or ISO 13485 preferred.
• Knowledge of Solidworks, Minitab, Excel, Power BI is desirable.
• Preferred knowledge in Lean Manufacturing, Six Sigma, Quality, etc.
• English proficiency.
Education
• Bachelor's degree in Industrial, Mechanical, Electromechanical Engineering, or any other engineering related to the position.
Competencies
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork