Senior Manufacturing Engineer

hace 2 semanas


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

About the position:

Responsibilities

  • Lead a dedicated group of engineers and technicians within the Project or Manufacturing Group.
  • Ensure engineers are fully integrated within the overall project and production support team.
  • Plan and implement training and development plans with subordinates.
  • Complete design and development projects through training and guidance of technicians.
  • Coach and mentor of team members.
  • Establish engineering goals and objectives that deliver results according to the business plan. Identify and establish permanent and effective technical/systems solutions to problems.
  • Consistently meet customer requirements and commitment to performance excellence and meet deadlines.
  • Prepare product and process reports by collecting, analyzing, and summarizing information and trends.
  • Defend compliance with Creganna Medical's systems and processes.
  • Identify and develop improvements to increase key metrics of the Service, Delivery, Quality and Cost process using Lean/6 sigma methodologies.
  • Research stateoftheart process technologies and evaluate the potential competitive advantage and cost benefit of the introduction.
  • Lead or guide projects in conjunction with other resource management (i.e., NPI, quality engineering, design assurance, R&D, and other crossfunctional departments) related to engineering. Work with the team to plan, coordinate and implement activities to support the successful launch of new products, including buy/purchase analysis, introduction of new processes and others. Develop/modify manufacturing processes by studying product requirements; research, design, modify and test manufacturing methods and equipment.
  • Maintain professional and technical knowledge by attending educational workshops; review of professional publications; personal networking; participating in professional societies.
  • Manage external relationships with key technology providers.
  • Manage a variable workload to meet operational requirements.
  • Ensure that all health, safety and environmental requirements are met.
  • Oversee and drive validation activities, including equipment IQ/OQ, process OQ/PQ, process characterization, validation of attribute/variable testing methods and associated documentation.
  • Indepth knowledge related to the links between the Master Validation Plan, pFMEA, dFMEA, risk management.

Education & Experience

  • Bachelor's degree in an Engineering field or equivalent, with 510 years of experience in a demanding highvolume production environment.
  • Knowledge of medical devices or systems of similar quality and manufacturing is a must.
  • Experienced CAD tool user, preferred SOLIDWORKS experience.
  • A proven ability to lead a production/technical troubleshootingfocused team with a proven track record of line configuration including equipment procurement and process development
  • Working knowledge of sigma and/or lean engineering principles with a proven track record in using and delivering results.
  • Statistical knowledge, including data analysis and the use of statistical software (JMP, Minitab, etc.).
  • Lean Six Sigma: Green Belt Certification Preferred
  • Must be fluent in English, both written and verbal, more than 80%

Competencies:

  • Values: Integrity, Accountability, Teamwork, Innovation


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