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    Imelda Sager Resume 2023

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    Imelda Sager
    Imelda Sager has over 30 years of experience in manufacturing, research and development, and quality assurance roles in the medical device industry. She is a team leader who improves processes and accomplishes tasks on deadline. Currently she is a production supervisor resolving issues and suggesting improvements at Tusker/Smith+Nephew. Previously she held roles with increasing responsibility at several medical device companies where she developed prototypes, managed production, trained staff, and ensured quality standards.

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    Imelda Sager Resume 2023

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    Imelda Sager
    7 views2 pages
    Imelda Sager has over 30 years of experience in manufacturing, research and development, and quality assurance roles in the medical device industry. She is a team leader who improves processes and accomplishes tasks on deadline. Currently she is a production supervisor resolving issues and suggesting improvements at Tusker/Smith+Nephew. Previously she held roles with increasing responsibility at several medical device companies where she developed prototypes, managed production, trained staff, and ensured quality standards.

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    Imelda Sager has over 30 years of experience in manufacturing, research and development, and quality assurance roles in the medical device industry. She is a team leader who improves processes and accomplishes tasks on deadline. Currently she is a production supervisor resolving issues and suggesting improvements at Tusker/Smith+Nephew. Previously she held roles with increasing responsibility at several medical device companies where she developed prototypes, managed production, trained staff, and ensured quality standards.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    7 views2 pages

    Imelda Sager Resume 2023

    Uploaded by

    Imelda Sager
    Imelda Sager has over 30 years of experience in manufacturing, research and development, and quality assurance roles in the medical device industry. She is a team leader who improves processes and accomplishes tasks on deadline. Currently she is a production supervisor resolving issues and suggesting improvements at Tusker/Smith+Nephew. Previously she held roles with increasing responsibility at several medical device companies where she developed prototypes, managed production, trained staff, and ensured quality standards.

    Copyright:

    © All Rights Reserved
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    of 2

    IMELDA SAGER

    CONTACT PROFILE
    Team leader with 30+ years in the medical device field within Manufacturing,
    (408)204-9010 Research & Development and Quality Assurance Departments. A hard-working
    professional, who demonstrates initiative by improving product processes,
    [email protected] accomplishing assigned tasks and meeting critical deadlines. My goal is to obtain a
    challenging position in the medical device industry.

     MICROSOFT EXCEL
    EXPERIENCE
     WORD Production Supervisor / R&D Technician
    2017 – Present | Tusker / Smith+Nephew
     POWERPOINT
    o Work with engineers and manufacturing engineers to resolve issues and suggest
     AGILE PRODUCT improvements.
    o Maintain work order records utilizing the QAD MRP System.
    LIFECYCLE o Maintain clean room integrity by using proper attire and adherence to clean room
    environment practices and procedures.
    MANAGEMENT
    o Support other departments as assigned.
    SOLUTION o Assist with laboratory testing protocols and document results.
    o Train new hire and other team members with new process.
     QAD MFGPRO o Work with engineer with design and development, building prototype
    o Perform design verification and validation.
    SOFTWARE o Transfer documents to manufacturing, and review Manufacturing Process Instruction
    o Familiar in issuing NCR
     MICROSOFT PUBLISHER o Highly familiar with all Tusker/ Smith-Nephew products and processes.

    EDUCATION Sr. Manufacturing Technician/Production Supervisor


    2010 – 2017 | Pivot Medical / Stryker
    o Manage and reports daily production results, including material usage waste and
    Bachelor of Science & downtime.
    Commerce: Business o Cooperate with Quality Control in maintaining quality standards, complying with
    appropriate corrective measures resolving deficiencies.
    Management o Manage personnel issues, including vacation approval, time card approval, daily and
    University of Cordilleras (Phillippines) weekly overtime.
    o Assist with development and implementation of policies.
    o Manage equipment and facility sanitation; initiates corrective action to resolve
    deficiency.
    o Maintains safety program and all required safety training for employees.
    o Maintain work order records utilizing the QAD MRP System.
    o Train new hire and other team members with new process.
    o Perform design verification and validation.
    o Transfer documents to manufacturing, and review Manufacturing Process Instruction
    o Work with engineer with design and development, build prototypes.
    o Assign daily work orders for Sub-assembly / Final Assembly and delegate to team
    members.
    Product Development / Sr. Operation Technician
    2009 - 2010 | TDC Medical
    o Prototype, product and process development: work with Engineers to develop quality
    and functional prototypes, products, and processes that contribute to the company
    objectives.
    o Offer excellent assembly knowledge, which includes processes and documentation.
    o Perform incoming inspection on receivable components (familiar with pin gage,
    calipers, snap gage and Ram Optical Instruments).
    o Familiar in creating document such MPI’s, LHR, BOM, DCO’s and Rework Instructions.
    o Familiar with MFG Pro System.
    o Perform shipping and receiving functions, manage inventory of all materials and
    components. Kitting work orders.
    o Perform design verification, PQ and OQ for product.
    o Perform surface treatment on metal and plastic components (i.e. Grit Blasted Wet &
    Dry, Sand Blasting).

    R&D Engineering Support/Sr. Manufacturing


    Engineering Technician
    2007 - 2009 | Benvenue Medical
    o Lead Design Verification, Design Validation and Clinical Trial Product Builds.
    o Train new hires with processes and documents, Initiate documentation for Benvenue
    product line (i.e. MPI, LHR, BOM), generate LHR format in MFGPro. Initiate and
    review DCO’s, Rework Instructions & NCR’s.
    o Manage engineering level documents and transfer/release to Document Control.
    o Support incoming inspections (First Article Inspection, Receiving Parts). Perform
    shipping and receiving functions. Manage inventory of all CER materials and
    components.
    o Offer excellent assembly knowledge, which includes processes and documentation.
    o Familiar with Titanium, Stainless Steel, Nitinol Wire. Familiar with engineering plastics
    such as Nylon, Peek, Polypropylene, Polycarbonate, ABS (Acrylonitrile Butadiene
    Styrene).
    o Familiar with engineering adhesives Cyanocrylae, Epoxy, and UV cure.
    o Takes initiative in making suggestions for process improvements ad fixtures.
    o Familiar with measuring instruments: Calipers, Snap gage, Micrometer, Ram Optical
    Instruments and Optical Comparator.
    o Basic machining skills (Drill press, Mill).

    Process Engineering Technician IV / Product Transfer


    Lead Technician – Costa Rica(Trainer)
    1997 - 2007 | ArthroCare
    o Prototype, product and process development: Work with Engineers to develop quality
    and functional prototypes, products, and process that contribute to company
    objectives.
    o Product Testing: work with Engineering to perform testing and development test
    methods and apparatus for evaluating the product quality and functionality.
    o Closely work with engineers in developing and implementing new manufacturing
    processes, create drawings, supporting validations and maintain laboratory notebook.
    o Highly familiar with technical features of all product lines.
    o Write MPI’s, test and validation protocols for products with minimal support from
    engineers. Validate new test methods and apparatus to evaluate safety and reliability
    of product.
    o Manage product transfer documents between Sunnyvale and Costa Rica facilities.
    o Train local and international assemblers on new product assembly and process
    updates.
    o Collaborate with engineers to design new fixtures, equipment and tooling.
    o Create ECN, releasing tools, fixtures, components drawings and do first article.
    o Familiar with engineering materials such as adhesives, heat shrink tubing and
    polymers.

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