Matt Reichelderfer

Continuous Improvement Manufacturing Manager at Shank's Extracts, Inc.
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Contact Information
us****@****om
(386) 825-5501
Location
Hershey, Pennsylvania, United States, US

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Experience

    • Continuous Improvement Manufacturing Manager
      • Apr 2021 - Present

      Lancaster, Pennsylvania, United States

    • United States
    • Packaging & Containers
    • 100 - 200 Employee
    • Quality Assurance Manager
      • May 2020 - Apr 2021

      York, Pennsylvania, United States

    • Interim Quality Manager
      • Jul 2020 - Sep 2020

      Lakeville, Minnesota, United States

    • United States
    • Packaging and Containers Manufacturing
    • 700 & Above Employee
    • Plant Quality Manager
      • Nov 2018 - Jan 2020

      Plant City, Florida • Safe Quality Foods Practitioner and Management Representative for the food safety system • Administered HACCP program, process risk program and Inspection Program • Responsible for all aspects of the food safety and quality system • Led reorganization of the quality department, with ultimate goal of increase in customer value added activities • Improved and led management review process monthly • Improved Internal Rejection System to be more streamlined and organized, reducing… Show more • Safe Quality Foods Practitioner and Management Representative for the food safety system • Administered HACCP program, process risk program and Inspection Program • Responsible for all aspects of the food safety and quality system • Led reorganization of the quality department, with ultimate goal of increase in customer value added activities • Improved and led management review process monthly • Improved Internal Rejection System to be more streamlined and organized, reducing wasteful inspection by 50% • Led teams from all levels of the organization to identify the true root cause of customer concerns and implement countermeasures • Implemented corporate procedure for complaint handling and resolution, which impacted the quality, sales and customer service departments • Implemented corporate procedure for issuance of letters of continuing guarantee and other required regulatory letters Show less

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Senior Lean Specialist, Americas
      • Aug 2017 - Nov 2018

      Tampa/St. Petersburg, Florida Area - Supervised team of 2 Lean Interns - Responsible for decreasing lead times through decrease of Work In Progress - Responsible for identifying and eliminating the sources of waste (TIM P WOOD) - Applied Six Sigma methodology to complex material movement problems - Lead Kaizen efforts at the plant level - Networked with other Lean Specialists to identify and implement best process practices

    • Senior Process Engineer
      • Feb 2016 - Aug 2017

      Jersey Shore, Pennsylvania • Supervised and Managed Engineering Technicians (program overhaul) • Performed installation qualification for Extruder #2 Move • Worked on 5S teams for several projects in the plant • Supported production by troubleshooting production problems • Facilitated implementation of several lean projects

    • Quality Engineer
      • Feb 2015 - Feb 2016

      Lock Haven, PA • Supervised team of Quality personnel to ensure Food Safety and Quality • Responsible for Quality System Improvements – Created Change Control Process, Overhauled NCR Process • Ensured Compliance to the Safe Quality Foods Standard Level III, 21CFR 110, PADEP Regulations • Administrated HACCP program, NCR Program, SCAR Program, Microbiologic Test Program, Inspection Program

    • Process Engineer
      • Aug 2013 - Feb 2015

      Lock Haven, PA • Implemented the 5S System of Organization • Utilized problem solving techniques to solve complex issues • Lead multi-functional teams to implement retrofits and product changes • Assisted with Injection Molding Supplier Troubleshooting and Start-ups

    • United States
    • Medical Equipment Manufacturing
    • 1 - 100 Employee
    • Engineer II
      • Aug 2011 - Aug 2013

      Elkton, MD • Planned, wrote and executed validation plans that conform to FDA QSR and ISO Requirements • Oversaw the installation and validation of new Injection Molding Press • Developed Scientific Molding Processes from ground up and validated • Worked within Medical Device Manufacturer Quality Systems (FDA QSR, ISO 13485)

    • Quality Engineer II
      • Jun 2007 - Aug 2011

      Elkton, MD • Led a group of Quality Associates to achieve goals set forth by the Quality Chief • Troubleshot Injection Molding Processes with Scientific Molding • Worked with other engineers to solve major production and design issues utilizing DOEs • Determined effects of product defects on end use • Designed and carried out tests to determine product defect hazards • Participated as Lead Auditor to ensure compliance to FDA QSR, ISO 13485 and other applicable standards • Conducted… Show more • Led a group of Quality Associates to achieve goals set forth by the Quality Chief • Troubleshot Injection Molding Processes with Scientific Molding • Worked with other engineers to solve major production and design issues utilizing DOEs • Determined effects of product defects on end use • Designed and carried out tests to determine product defect hazards • Participated as Lead Auditor to ensure compliance to FDA QSR, ISO 13485 and other applicable standards • Conducted Corrective Action/Preventative Action • Trained New Quality Engineers in regards to roles, responsibilities and quality systems • Created the Statistical Process Control procedure in use at the Elkton, MD site

    • Operator II
      • Jun 2006 - Jun 2007

      Elkton, MD

Education

  • Frostburg State University
    Master of Business Administration (M.B.A.)
    2014 - 2017
  • Pennsylvania College of Technology
    Bachelor of Science (B.S.), Plastics and Polymer Engineering Technology
    2002 - 2006

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