Senior Process Development Engineer

hace 2 meses


San Francisco, Heredia, Costa Rica Te Connectivity A tiempo completo

**Job Summary:**

As a Senior Process Development Engineer at Te Connectivity, you will be responsible for developing and optimizing manufacturing processes to ensure high-quality products. Your background should include experience in statistical techniques, product cost components, and installation/validation activities for production lines. Additionally, you should have a strong understanding of ISO 13485 and continuous improvement methodologies. You will work closely with the team to identify areas for improvement and implement changes to meet regulatory requirements.

**Key Responsibilities:**

  • Develop and optimize manufacturing processes to ensure high-quality products
  • Analyze equipment data, trends, and performance to assure correct lifecycle management
  • Identify and mitigate risks associated to equipment technical knowledge, spares availability and external technical service
  • Evaluate the financial, process or quality impact, derived from product & process changes
  • Assure that production lines output meet the specifications of the product
  • Able to navigate and execute activities on manufacturing systems for example, update routers, BOM's or to generate new part numbers
  • Coordinate the activities related to new part numbers implementation
  • Maintain MP's current and compliant to regulations
  • Supports DL's & IDL's training process
  • Participate in the identification and investigation of Non-conforming products
  • Use Root cause problem solving techniques to identify and eliminate causes, implements controls and define preventive activities
  • Lead or support CAPA investigation processes, or exception documents such as complaints investigations
  • Identify and implement continuous improvement projects for any of the main key areas: safety, quality, production and cost, using the appropriate project management tools
  • May supervise and provide technical assistance to exempt and non-exempt personnel, being accountable for their correct training and performance management
  • Provide inputs for the departmental budget preparation

**Requirements:**

  • Bachelor's Degree in Mechanical/ Material or equivalent discipline. Plus 3-5 years prior experience in medical devices manufacturing.
  • 6+ years of manufacturing/process development experience
  • Computer software knowledge (Microsoft Word, Excel, Power Point).
  • Experience or knowledge in Grinding process, Overmoulding and extrusion is a plus.
  • Experience with continuous improvement methodologies. Such as lean manufacturing techniques, value stream mapping, or similar.
  • Knowledge of ISO 13485 is required.
  • Experience leading validation plans for medical industry products and processes and leading root cause problem solving methodologies.
  • Experience in project management.
  • Advance command of English (written and speaking). Required

**Competencies:**

Values: Integrity, Accountability, Teamwork, Innovation



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