Angela Cancino

Experience

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  Medimexico

  Dec 2005 - Apr 2007

  Manufacturing Engineer

  Create proceduresValidations

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  Smiths Medical

  Apr 2007 - Jul 2011

  Manufacturing Engineer

  Create BOMWork InstructionsValidations

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  Nypro, A Jabil Company

  Jul 2011 - Jun 2019

  • Create inspections plans and coordinate inspections for incoming material.• Responsible for Transferring Material from Rochester to Tijuana.• Disposition and released of non-conforming material. Experience and understanding Quality System Regulation (QSR 21 CFR 820), ISO 13485:2003, ISO 9001 including documentation for product release and quality assurance: Manufacturing and Quality Inspection Procedures, Process and equipment Validations, New Product Introduction, First Article Inspection, FAT, DMAIC, Problem Solving Tools, FMEA, Process Map, Flow Charts, Gage R&R, Inspection Sampling Plan, 8D’s, Six Sigma Tools, Business continuity Programs, Lean Manufacturing. Create BOMCost reduction projects.Train operators.New product implementation.Create work instructions.Creation of Fixtures.Validations

  • Incoming Inspection Supervisor

    Jan 2018 - Jun 2019

  • Sr. Quality Engineer

    Aug 2013 - Jun 2019

  • Manufacturing Engineer

    Jul 2011 - Jun 2019
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  Smiths Medical

  Jun 2019 - Jul 2020

  Principal Quality Engineer

  • Responsible to coordinate daily Quality Engineers activities – 5 QEs.• Responsible to execute, approve protocols and reports for process, equipment and software validations including Master Validation Plans, Test method validation, IQ, OQ and PQ.• Areas of responsibility: Quality Engineers and In Process Quality Inspection.

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  NEOTech

  Jul 2020 - Apr 2022

  Quality Manager

  • Responsible for implement Quality activities and strategies to comply with Medical, electronic regulations and customer requirements for Harness and PCBS assemblies based on ISO 13485 and IPC regulations.• Active participation as Audit Room Manager, War Room Manager and SME on MDSAP certification and on several Customer audits based on ISO 13485:2016, 21 CFR 820 and ISO 9000:2015 for Tijuana and San Marcos US Facilities. • Areas of responsibility: Quality Engineers, Document Control Department, Training Department, In-Process Quality Inspection and Supervisors, Incoming Inspection and Calibration Department. Show less

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  Scantibodies Laboratory, Inc

  Jul 2022 - now

  • Sr. Global Quality Assurance Manager

    Oct 2024 - now

  • Regulatory Affairs Manager

    Jul 2022 - now