Curtis Griffy (Lion), Msm, Pmp Email and Phone Number
Saint Paul, MN, US
Curtis Griffy (Lion), Msm, Pmp's Location
Greater Minneapolis-St. Paul Area, United States, United States
Curtis Griffy (Lion), Msm, Pmp's Contact Details
Curtis Griffy (Lion), Msm, Pmp work email
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Curtis Griffy (Lion), Msm, Pmp personal email
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Curtis Griffy (Lion), Msm, Pmp phone numbers
About Curtis Griffy (Lion), Msm, Pmp
WHAT I DO IN 15 WORDS OR LESSI lead YOUR project TEAM to complete YOUR strategic projects WITHOUT Loss Of Valuable TimeEssentially,I allow you to focus on running other parts of the business INSTEAD of you having to stay on top of the project teams. and I eliminate your STRESS of leading the team to make constant progress.WHO DO I WORK WITH? CEOs, Presidents, Vice Presidents and DirectorsWANT AN EXAMPLE?I led 3 Class II R & D Medical Device Projects simultaneously that completed by the new regulation enforcement date to protect 10s of millions of dollars revenue stream from dropping to zero. Well, I know what you are thinking.Well, Curtis how did you do this?How about this answer?I use Expert techniques to organize project work, build the project schedule, use statistical techniques following the traditional project management process. This will give YOU the most realistic project schedule. It will give You the answer to Your question of how likely the project will finish on a given date. If you would rather use the Agile process for a defined completion date with as many product features the team can fit in by that defined date, I can facillated the team using this process too.I utilize expert people skills to inspire the project team and hold them accountable to their commitments. WHAT OTHERS SAY:“I worked with Curtis Griffy at Smiths-Medical on the Medfusion 4000 test team. During my time working with him, I felt as though I was being mentored by an industry expert. Curtis has the great ability to manage the big picture without losing his incredible attention to detail. He is patient, gracious, humble, knowledgeable, resourceful… I can’t imagine a scenario when his input would not be greatly appreciated. He is a true project management professional. I would gladly welcome any opportunity to work with Curtis again in the future.” Thomas Doyle.If you want, then please (Call 651-261-0814 / Email Curtis.Griffy@Problem-Busters.com) me to see if we’re a good fit to work together.”
Curtis Griffy (Lion), Msm, Pmp's Current Company Details
Curtis Griffy (Lion), Msm, Pmp Work Experience Details
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Consultant - Project ManagerRqm+Saint Paul, Mn, Us
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FounderReie Llc Dec 2018 - PresentBoss Bio: Curtis Griffy, REIE LLCGreetings! I am Curtis, dedicated to leading my business with integrity and Christian values. My expertise lies in the realm of vacant land, where I specialize in assisting landowners to effectively convert their properties into cash. Whether you're looking to sell undeveloped land or seeking a parcel for building a home or recreational use, I am here to guide you through every step of the process.With a deep commitment to ethical business practices and a passion for real estate, I strive to provide personalized solutions that meet the unique needs of each client. My goal is not only to facilitate transactions but also to foster lasting relationships built on trust and mutual respect.If you're ready to explore the possibilities of vacant land, whether for investment, development, or personal enjoyment, I invite you to connect with me. Together, we can turn your land aspirations into reality, grounded in principles that matter.
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Chief Executive OfficerFund Your Offer May 2022 - PresentHello. My name is Curtis and I’m with Fund Your Offer. We’re a nationwide private money lender with more money than deals. I’m excited about our new loan program that offers 100% financing for fix and flip loans. This does include 100% of the purchase price, 100% of rehab, and even 100% of closing costs- not to exceed 70% of the ARV. This is for non-owner-occupied residential deals, up to 4 units. All loans are for investment purposes only. If you or anyone you know could use 100% financing, please get back to me. We also offer a $500 dollar referral fee on every referred closed loan. Check out our website www.fund-your-offer.com
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Course InstructorIcert Global Dec 2018 - PresentHouston, Texas, UsWHAT I DO: I instruct students in a topic area from my skill set to gain the knowledge they can use in their work.ASSIGNED PROJECT: Teach Project Management fundamentals class for the student WHY IT MATTERS: Individuals must have 35 hours of classroom project management training to meet one of the requirements to apply to take the PMP exam.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
Founder || Project | Program ManagerLeadership For Project | Program Operations Management In The Greater Minneapolis-St. Paul Area 2015 - PresentAttending networking eventsResearching Industry LeadersTracking Industry TrendsParticipating in Industry Discussions
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Consultant - Project ManagerRqm+ Oct 2021 - PresentMonroeville, Pa, UsWHAT I DO: The client has assigned me to another project to operate as a Project Manager. The project is to build, mentor 2 new team members, and lead them to assess 276 software systems to determine if there are compliant validation packages including the System Risk Classification (SRC) document (determines if it's a GxP system or regulated by other regulations). If a system is found with a non-compliant SRC to the SOP, then a new SRC will be created and released. After all needed SRCs are created, then the team will do any needed remediation validation to close the gap of a non-compliant package.
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Consultant - Business AnalystRqm+ Dec 2019 - Oct 2021Monroeville, Pa, UsWHAT I DO: The client has assigned me to another project to operate as a BA. The project is a web-based training application Validation. I am charged with writing user requirements, user test cases and tracing between the two in HP Quality Center. Then, I have to create other validation documents that include Business Risk Assessment, Configuration Inventory, eRIM (electronic record Information Management) document which covers part of FDA 21 CFR Part 11, a data privacy document to document compliance to GDPR and CCPA. I will be creating a complete validation set of documents compliant to the company's SOP.
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Sr It Compliance AnalystMaetrics Jul 2019 - Dec 2019Monroeville, Pa, UsWHAT I DO: I assess documentation of released business quality classified software. The client company decided to engage me for another project initially for 3 months, but the amount of project work needed to complete could cause the need to extend me until the end of December. The first phase of this project is to assess an estimated 375 software systems for another business unit to see if a software risk classification was done and was it done correctly. If the system does not have the risk classification or was inadequate, I will author a replacement or new one. I will have it reviewed by the appropriate stakeholders. Add it to the document repository and route it to be officially approved. If I find any systems that were not validated, then I submit a request to the appropriate IT group to write the validation document set to meet the level of validation required based on the software risk classification, perform the validation and write the validation report to meet the requirements of the company SOP. -
Senior It Compliance AnalystMaetrics Apr 2019 - Jul 2019Monroeville, Pa, UsWHAT I DO: I perform IT Compliance Analysis on a business integration project. I analyze Computerized System/Software documentation such as System Risk Classification, requirements documents, validation plans, test plans that were compliant a Division Quality System SOP for gaps to transition them to be compliant with the Global Computerized System/Software Life Cycle Quality System SOP. For gaps found, request IT owners to fill the gaps. This effort falls under the FDA QUALITY SYSTEM REGULATION 21 CFR 820.70(i). The systems include SAP, systems that handle the device history record, systems that handle clinical trial data including data protected by HIPPA, the system for handling complaint information, and systems that handle privacy data. WHY IT MATTERS: The reputation of the business is on the line from bad press because your organization has had a Warning Letter Issued from the FDA for operating outside of compliance of your Quality Plan. The impact of this is a drop in product sales due to the potential customer running scared from the fear of poor quality. In addition, the FDA could levy a significant fine for your company.RESULT: 70 Systems Assessed. 19 were dropped because Inventory said they were Quality Systems, but after assessing the Risk Classifications they were classified as non-quality systems making them out of scope for the gap assessment. The remaining systems I assessed for gaps. Only 67% of the remaining systems had gap issues. The issues were missing validation deliverables. Missing validation deliverables can be grounds for an FDA 483 Warning Letter. There were 2 different deliverables but commonly missing on 9 systems resulting in a CAPA being initiated. WHO I WORK WITH: Division Vice President, IT Directors, Quality Directors, IT Managers, Quality Managers, SQA and SME's.READY TO TALK? Reach out to me directly here on LinkedIn, email me at Curtis.Griffy@gnaweb.net, or call me direct at 651-261-0814
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Project Lead Validation Engineer | ConsultantEntegee May 2016 - Sep 2016Burlington, Ma, UsWHAT I DO: I bring Medical Device clients analytical laboratory, equipment and test methods used for incoming inspection to follow FDA regulations through validation. ASSIGNED PROJECT: Validate the Medical Adhesive Bond Strength Test and Associated Equipment.I design Validation Plans for Test Methods using a Gage R & R Study. My findings of the Analysis of the Current State (below) it was clear I needed to verify the quality of the test specimen preparation before trying to validate the test method. I designed an experiment based on the FULL FACTORIAL Design using Minitab. To address the equipment traceability issues, I ordered new equipment with calibration certificates.WHY IT MATTERS: Boston Scientific acquired the Men’s Health Division of American Medical Systems that had and FDA Warning Letter with one of the deficiencies listed that the equipment and test methods used in the analytical laboratory did not comply with FDA regulations that it must be validated for a CAPA. WHO I WORK WITH: I work with lab technicians, the lab manager, and Remediation Project Manager.ANALYSIS OF CURRENT STATE: I confirmed there was no traceability of calibration equipment used for sample preparation. I identified there was not a drawing or specification for the material to use for test sample preparation. I identified discrepancies in the sample preparation instructions and test method. I observed variation in sample preparation by the laboratory technician.MY EXPERIMENT RESULTS: Analyzing the data with Minitab the thickness of the adhesive in the joint varied tremendously as indicated by a Cpk of 0.15. Thus, the value of the bond strength measurement would be highly variable due to the sample preparation thus impossible to determine if the adhesive bond strength met spec or not. Management decided to eliminate the use of this test.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
WebmasterGriffy & Associates Sep 1999 - May 2016WHAT I DO: I help startups, small business and non-profits achieve visibility on their product and or service by providing website design and hosting services.WHO I WORK WITH: I partner with startups, small businesses or non-profits including★ Owner★ Marketing Director★ Sales Director★ Communications DirectorWHY IT WORKS: When you partner with Griffy & Associates you get the most efficient, effective and service that a startup, small business or non-profit is looking for right now.WHAT MAKES US DIFFERENT: Our quoting and pricing structure turns the rules on a quote for the cost of a repair at a car dealer on its head and probably many other businesses as well. We also have unique payment terms for improving the efficiency of your marketing capital.HOW IT WORKS: We start with a free design consultation. We likely will meet via phone to discuss your needs. Then, we sit down with you face to face with a pencil/pen and sketch pad to design the framework of your website to give us the starting point for the design. Then publish the start of your web pages online so you can watch as the design progresses. READY TO TALK? Reach out to me directly here on LinkedIn, email me at Curtis.Griffy@gnaweb.net with the subject line set to your website URL, visit us online at www.gnaweb.net or call me directly at 651-261-0814.
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Software Qa Engineer/Project Specialist | ConsultantAerotek Contractor At Minnetronix Dec 2014 - Jul 2015Hanover, Maryland, UsWHAT I DO: I validate Medical Device Clients device operation embedded software and various other electronic engineer tasks.*Embedded Software Validation ProjectI was tasked to run the existing or newly updated test protocols to show the software operated per the software requirements. I found many issues that needed to be addressed in the software protocols which I recorded for the next round of protocol updates. I converted a manual test to an automated one that reduced its execution time by 50%. After a few rounds of test runs, I report the bugs and developers fix, the software was shown to be validated to the defined software requirements. Participated in Agile Standup Meetings.*Heat Rise StudyI designed a heat rise study on the controller’s internal NiMH battery and other components for the heart pump. I used a thermal imaging camera to identify where to attach thermocouples. I discovered the internal temperature climbed to a temperature that exceeded the spec for efficient charging battery.*Low Battery Alarm Test Fixture ValidationI added automation to the test fixture validation plan. This it reduced the test time by 5 days since now it could be run overnight unattended.Diode Issue PerformanceDesign an automated test to compare different diode grades over the operating conditions of the pump controller to determine if using the higher cost diodes would provide improved performance for the cost.WHY IT MATTERS: Minnetronix was contracted with their client to update the operation embedded software design for a Class III implantable ventricular assist heart pump to fix issues on a CAPA that caused the client to get an FDA Warning Letter.WHO I WORK WITH: Software Update Project Test Lead, Director of Design Quality Assurance and embedded software developers.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
Program ManagerSmiths Medical Dec 2012 - Nov 2014San Clemente, California, UsWHAT I DO: I lead Medical Device ROHS (Restricted Hazardous Substances) compliance transformation and obsolescence Design Engineering Projects.The projects in the Program I was to lead are Medfusion Syringe Infusion Pump (Budget $1,500,000, a new product launch for EU), Pulse Oximeter (Budget $525,000), Patient Monitor (Budget $637,000), CADD (Budget $800,000) and Legacy (Budget $1,200,000) Ambulatory Infusion Pumps. And, all their accessories. Each of the products also had obsolete components that needed to be replaced before running out of inventory. I influenced Environmental Engineering to define an SOP that the engineering teams need to follow to transform products to be ROHS compliant.I create MS Project schedules with team collaboration. I manage each project issues list, enhanced and manage the Risk Registers. I manage the Design History File and the budget for all projects. I met the with Regulatory weekly. I create PowerPoint Status Slides for monthly director and Quarterly Executive Staff meetings.PROGRAM RESULT: All but the Medfusion project were completed by the EU enforcement date. The Medfusion Project engineers were diverted to a field issue for about 12 weeks. When they rejoined the project, we crashed the schedule for the new product launch into the EU resulting in a one-month delay. All projects completed within budget.WHY IT MATTERS: The product's sales produce a double-digit million-dollar revenue stream from the EU. The medical devices had to be transformed to be ROHS compliant by 7/22/14 enforcement date to ensure they are not blocked from entering the EU to be sold.WHO I WORK WITH: Electrical Engineers, Mechanical Engineers, Manufacturing Engineers, the Supply Chain, Marketing, Labeling, Design Assurance, Regulatory agents, Vice Presidents, and President. The Program staff count was 55.READY TO TALK? Reach out to me directly here on LinkedIn, email me at Curtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
Project Manager | Embedded Software Validation Team LeadSmiths Medical Apr 2009 - Dec 2012San Clemente, California, UsWHAT I DO: I am the Project Manager Embedded Software Test Leader that was converted from a consultant to an employee and charged to lead the embedded software testing effort for the Medfusion 4000 Syringe Infusion Pump.*Configuration Management Tools used were DOORS, Subversion and Mantis.*Create/update the software validation project schedule in collaboration with the test team.*Reviewer and co-signer for formal software requirements.*Delegate the rewrite, update or new test cases/procedures to the test team.*Led Agile Standup Meetings.*Responsible Author of software validation plan, test procedures, software validation report release.*After 8 months working with the Indian test team, I requested the team be terminated from performing the software validation for the Medfusion 3500. I could not trust their test results.*The Director of the PMO had his program managers go through a brought in house 35 hours of class room training that is required for the PMP certification. After the program managers were trained I co-lead and PMP study group to help the program managers for the PMP exam.SOFTWARE VALIDATION RESULTS:*Medfusion 4000 was completed after 3 test regression runs. The Medfusion 4000 was in the market for 2 years with no reported software issues.*Medfusion 3500 was validated and after 2 regression test runs, it was released.WHY IT MATTERS: Smiths Medical needed to release the Medfusion 4000 software for the FDA Submission and Approval to market new model pump.WHO I WORK WITH: Software Embedded Software Developers, Development Manager, Embedded Software Project Engineer, Software Test Engineers, Software Test Technicians, Marketing, Clinical Registered Nurse, Pharmacist, Program Manager, Software Validation Manager, Design Assurance, and Regulatory; a Remote Software Test Lead and team in India.READY TO TALK? Reach out to me directly here on LinkedIn, email me at Curtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
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Co-Chairman, Community Outreach PmoProject Management Institute - Minnesota Chapter Jan 2008 - Aug 2010Minneapolis, Mn, UsWHAT I DO: I volunteer for the Minnesota Chapter of the Project Management Institute taking the role of Co-Chairman of the Community Outreach function of the Chapter. The Co-Chairman is one of the Operations Board members.*I direct two of the four Community Outreach Program Managers*I manage the Community Outreach budget - $42,000*I recruit project managers to open Chapter Monthly Dinner/Training Meetings in new cities/states such as Duluth and Moorehead-Fargo.*I host monthly Community Outreach Team MeetingsWHY IT MATTERS: Part of the Charter of the Chapter is to create projects that contribute to the Community using our Project Management Skills either directly or partnering with other organization that contributes to the community. Community Outreach contributes to several sectors.WHO I WORK WITH: I partner with other Community Outreach Volunteers.*Operations Board*Community Outreach Program Managers* Community Outreach Project ManagersWHAT OTHERS SAY:“2008. Curtis provided great direction and strong leadership as the 2008 Community Outreach Co-Chair. Curtis was responsible for the PMI MN Outreach and Community Services programs. He was able to oversee at a high level, manage at a detail level and also do what needed to be done. He has a keen sense of his volunteer team’s capabilities and no-nonsense approach to getting things done. I look forward to working with Curtis in 2009. Matt Mehring, Director Project Management Institute Minnesota Chapter.”READY TO TALK? Reach out to me directly here on LinkedIn, email me at Curtis.Griffy@gnaweb.net, or call me direct on 651-261-0814. -
Project Manager | Lead Test Embedded Software | ConsultantSwat Solutions May 2008 - Apr 2009St. Louis Park, Mn., UsWHAT I DO: I create and update the software validation test schedule. I design new/update Blackbox and Whitebox tests. I review the software issues found by the testers. I define the regression test list a formal validation run that finds more software issues. I role up my sleeves and assist with executing the test procedures during a dry run and the formal validation run. I author the formal validation report and review it with Design Assurance for formal sign off.WHO I WORK WITH:*Test team members*Software Development Engineers* Software Project Engineer*Software Development Manager*Design Assurance*Clinical nurse and pharmacist *Regulatory AgentWHY IT WORKS: It takes a highly trained project management professional with a deep software engineering background.WHAT MAKES ME DIFFERENT: For Project Management, I have been trained by the Best. For the Technical Software Test Lead, I have about 15 years of software development. WHAT OTHERS SAY: “Curtis led several software development test efforts for me at Smiths Medical. He is an extremely hard worker and gets along with his co-workers very well. He puts an emphasis on quality both of his own work and that of his team members.” My manager, David Carpenter.“I worked with Curtis Griffy at Smiths-Medical on the Medfusion 4000 test team. During my time working with him, I felt as though I was being mentored by an industry expert. Curtis has the great ability to manage the big picture without losing his incredible attention to detail. He is patient, gracious, humble, knowledgeable, resourceful… I can’t imagine a scenario when his input would not be greatly appreciated. He is a true project management professional. I would gladly welcome any opportunity to work with Curtis again in the future.” One of my software test team members, Thomas Doyle.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
Principal Engineer | Project Lead TestBoston Scientific Crm Formally Guidant Corp Oct 2001 - Nov 2007Marlborough, Ma, UsWHAT I DO: I use my deep electrical engineering and leadership background to solve problems. For example, in Supplier Quality using my deep statistic background identify vendor quality issues that cause our incoming inspection to reject their product. Then, recommend additional quality improvements for their process they go ahead and adopt.I work to assist in closing CAPAs.I contribute to FMEAs to get them complete ahead of schedule for FDA submission.I consult with another engineer on his RF test system design.I perform validation on the first RF test application.I reduce the test time by 80% for defibrillator high voltage modules by designing a unique fixture and using C++.I identify a replacement and procure a new test system.I use my project management skill to lead 5 engineers for 5 new test software projects on the new test system.WHO I WORK WITH: Electrical Engineers, Technical Writers, Schematic and Printed Circuit Board Engineers, Mechanical Engineers, Process; Manufacturing Engineers and technicians.WHAT MAKES ME DIFFERENT: I am a fast learner. I design creative solutions.WHAT OTHERS SAY: “Curtis is a very quality-driven, detail-oriented engineer, which made him a great asset in the medical electronics field.” One of my co-engineers, Mark Buzicky“I worked with Curtis Griffy at Boston Scientific CRM on a rather large and time intense project to test and qualify the components and assemblies required to manufacture a next-generation cardiac pacemaker/defibrillator. He was always very easy to talk with and I enjoyed working with him. At the principle engineering level, Curtis got results in on time and was always there to provide the answers to some very difficult questions. I would work with him anytime, anywhere, and place.” My tech writer, Stephen KnowlenREADY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
Senior Engineer | Test Engineer | ConsultantAerotek Engineering Oct 1999 - Oct 2001Hanover, Maryland, UsWHAT I DO: Is develop mixed signal and high voltage module test applications on the LTX Mixed Signal Test System.I design the test fixture and develop mixed-signal test application for dual leaded chip carrier that has a digital and analog ICs within it. By 3 months into this assignment, I had 90% of the test application complete before attending the 3 weeks training on the complex LTX test system. I went on to complete the application on time per the project manager’s schedule.I design the test fixture and the high voltage (800V) test application for the defibrillator high voltage output module on time per the project manager’s schedule.WHO I WORK WITH: Electrical Engineers, Technical Writers, Schematic and Printed Circuit Board Engineers, Mechanical Engineers, Process; Manufacturing Engineers and technicians.WHAT MAKES ME DIFFERENT: I am a fast learner. I design creative solutions.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
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Application Engineer | Fcc Compliance EngineerRelm Communications 1992 - Mar 1997WHAT I DO: I hold contracted 3rd party offshore product design firms accountable to our product design and quality requirements. I design new configurations for new applications for our products. I transform customer complaints into customer praises.I work with a design firm rep for and RF design companies in China and Japan on two $3,000,000 handheld business band two-way radio model lines one called PT and the other WHS.I took on the Project Manager/Technical lead for a high-performance business band two-way radio to be designed by a 3rd party in Israel.I performed RF testing on the two radio models against our requirements and the FCC requirements to be granted Type Approval so they could be sold in the United States.I performed environmental testing to the operating range -25 to + 60 F spec.I perform embedded software testing.I cause vendors to ask for mercy.I create FCC Submissions.I get FCC Type Acceptances granted on 6 business handheld two-way radio models.I designed a system application using 3rd party singling system for handheld two-way radios and a business band mobile radio to serve as a base station for a customer in Brazil.I was given a customer issue with the new PT radios to solve. After several attempts to diagnose over the telephone and sending the equipment back and forth, the solution was not found. I told my boss the VP of Engineering that I must go to the customer site to solve the problem. In three days I had everything working and the customer was happy. The customer responded with the letter attached.WHO I WORK WITH: RF Electrical Engineers, Embedded Software Engineers, Technicians, Tech Writers, FCC, Marketing, CustomersWHAT MAKES ME DIFFERENT: I accept nothing but the best quality. I perform testing to the extremes. I am passionate about elating customers.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
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Electrical Engineer | Six Sigma Problem Solving Team LeaderMotorola Jan 1988 - Sep 1992Chicago, Illinois, UsWHAT I DO: Design tuning application using Pascal to operate IEEE-488 controlled RF test equipment to assist factory staff to properly perform the tuning of the receiver and transmitter in handheld business band two-way radios.Design two-way radio test application using Pascal to operate IEEE-488 controlled RF test equipment for the System Test to check the radio RF performance to specification.Design a two-way radio Quality Audit test application using Pascal to operate IEEE-488 controlled RF test equipment.I took an advanced IEEE-488 programming class from a Hewlett Packard Expert then applied what I learned to revise my RF Tuning, System Test and Quality Audit application to reduce test time resulting in an annual savings of over $1,000,000.Raised our Statistical Analysis capability by purchasing and configuring RS1/QCA statistics package on a UNIX workstation. This gave us more robust tools and reduced our analysis times by 50%.Trained in Six Sigma by the Motorola authors. I took these skills to lead a team using Six Sigma to solve a problem the plagued the factory since the first prototype was built. I create PowerPoint Slides to communicate what the team did. We were recognized as the top team in our factory. We went to compete with other teams in our division. We were selected as the most successful Six Sigma team of the Division. We then were required to travel to Maui, Hawaii to share our success and collaborate with the other top teams from other Motorola locations around the globe.WHO I WORK WITH: RF Design Engineers, Marketing, RF technicians, Quality Auditors, and general manufacturing operators.WHAT MAKES ME DIFFERENT: I inspire and lead teams to strive to be second to none. I look outside the box to learn about potential game changer solutions then go after them to implement to gain significant results.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814. -
Test Engineer | In-Circuit TestRegency Electronics 1982 - 1988WHAT I DO: I seek and implement new methods to automate design transfer to manufacturing to reduce implementation time.I work with the CAD Manager to create CAD scripts to export x-y data for the programming of the CNC axial printed circuit board (PCB) parts assembly machine for product printed circuit boards for minimum component placement time.I work with the CAD Manager to create CAD scripts to export x-y data for test point locations for the test points for the in-circuit test fixture for using a CNC to drill the test fixture plates.I acquired an automated in-circuit test program generator for our Zentel testers to cut in-circuit test program development time.I work with the CAD Manager to create CAD scripts to export the printed circuit component list with part tolerances to be used as input the automated in-circuit test program generator.I design “C” programs to calculate the receiver spurious response frequencies for RF testing to replace manually sweeping the RF generator from 1 Hz to 1 GHz looking for spurious responses cutting test time by 300%.WHO I WORK WITH: CAD Manager, CAD Designer, Mechanical Engineer, RF Engineer, manufacturing test operators, and vendors.WHAT MAKES ME DIFFERENT: I am always seeking learning opportunities that I can transform into actions for process improvement, quality improvement, and cost savings. I can effectively collaborate with anyone in the organization for improvement opportunities.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
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New Product Development Engineering Technician | Marine Two-Way RadioRegency Electronics 1980 - 1982New Product Development Engineering Technician | Marine Two-way RadioCompany NameRegency ElectronicsDates Employed1980 – 1982 Employment Duration2 yrsLocationIndianapolis, Indiana• Measured regulatory required transceiver parametrics for submission report for regulatory approval to market in Europe• Revised design on high end marine transceiver that had a stop marketing order from the Department of Canada. Resubmitted revised design performance data to the Department of Canada. Transceiver was re-approved for marketing in Canada.• Diagnosed and repaired Zehntel ATE In-Circuit Testers purchased from used equipment market. Created two functioning testers from three purchased as non-working machines for parts.WHAT I DO: I am the two-way marine radio RF Engineering Technician to assist the RF Design Engineer in developing a new marine radio product line for outside of the United States.I etch and drill prototype circuit boards for the new marine radios. I perform RF parametric testing for regulatory submission to the various countries targeted the market the new radios in.Department of Canada pulled our authorization to market our marine radio with the built-in direction finder due to un-allowed RF emission from the radios. I made a design change to eliminate the problem and resubmitted to Canada and got our authorization reinstated to sell the radio in Canada.I converted three scrap Zentel In-Circuit testers the company purchased into two fully functional testers for the Florida manufacturing plant.WHO I WORK WITH: RF Engineers, prototype assembler, Bill of Material AdministratorWHAT MAKES ME DIFFERENT: Passionate to learn what it takes to be an RF EngineerREADY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
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Electronic Technician | ManufacturingRegency Electronics 1979 - 1980WHAT I DO: I diagnose the root cause of the police scanner radios defects that have its receiver fail to tune up per specification on the manufacturing floor. I work on work production line rejects and quality test rejects after burn in.I would pinpoint the defective component in the radio then have my repair person replace the bad component. In a typical day, I would diagnose and have repaired 90 units to keep the repair person buried. Initially I started as an intern and this level of performance caused the plant manager to offer me a full-time job.I built the in-circuit test fixtures for the test engineer.WHO I WORK WITH: Plant Manager, production line tuning staff, test engineer and quality testers.WHAT MAKES ME DIFFERENT: I am driven to be an over achiever to make significant impacts.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
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Shop Foreman | Machnist | Molding Press Repair TechnicianL.B. Griffy And Sons, Inc. Apr 1977 - Dec 1978Our company was a plastic injection molding business with an in-house machine shop to build and maintain plastic injection molds. The customer base was industrial and medical supplies.Our company was a plastic injection molding business with an in-house machine shop to build and maintain plastic injection molds. The customer base was industrial and medical supplies.WHAT I DO: I wear many hats in our Company -shop foreman, machinist, job setup and molding machine repair technician.I oversaw the work and helped the 5 molding press operators run the plastic injection molding machines.I ran the Bridgeport Milling Machine, drill press, lathe and Surface Grinder to help my father build new or repair molds for our customers.I diagnosed electrical and hydraulic problems that would occur on the injection molding machines.I did molding machine setup switching molds and connected cooling.When a job needed colored plastic, I would die the raw material to the color the customer required.I managed the stockroom using the fork lift as needed.WHO I WORK WITH: President – aka my dad, molding press operators.WHAT MAKES ME DIFFERENT: I am teachable and willing to learn new things that are completely different from what I already have knowledge in.READY TO TALK? Reach out to me directly here on LinkedIn, email me atCurtis.Griffy@gnaweb.net, or call me direct at 651-261-0814.
Curtis Griffy (Lion), Msm, Pmp Skills
Cross Functional Team Leadership
Program Management
Testing
Project Management
Management
Leadership
Pmp
Strategy
Ms Project
Quality Assurance
Medical Devices
Manufacturing
Sdlc
Validation
Visio
Fda
Analysis
Electronics
Product Development
Engineering
Quality System
Requirements Analysis
Test Planning
Iso 13485
Embedded Software
Software Documentation
Process Improvement
Microsoft Project
Software Development
Fmea
Software Quality Assurance
Continuous Improvement
Unix
Six Sigma
Lean Manufacturing
Team Leadership
Project Planning
Process Engineering
R&d
Data Analysis
Consulting
C
Integration
Process Simulation
Design Control
Curtis Griffy (Lion), Msm, Pmp Education Details
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Colorado Technical UniversityProject Management -
Purdue UniversityElectrical Engineering Technology
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Franklin Central High SchoolCollege Prep
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Dale CarnegieLeadership
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Professional Development Days Pmi- MnProject Management
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Professional Development Days Pmi- Mn
Frequently Asked Questions about Curtis Griffy (Lion), Msm, Pmp
What company does Curtis Griffy (Lion), Msm, Pmp work for?
Curtis Griffy (Lion), Msm, Pmp works for Rqm+
What is Curtis Griffy (Lion), Msm, Pmp's role at the current company?
Curtis Griffy (Lion), Msm, Pmp's current role is Consultant - Project Manager.
What is Curtis Griffy (Lion), Msm, Pmp's email address?
Curtis Griffy (Lion), Msm, Pmp's email address is cu****@****web.net
What is Curtis Griffy (Lion), Msm, Pmp's direct phone number?
Curtis Griffy (Lion), Msm, Pmp's direct phone number is +165126*****
What schools did Curtis Griffy (Lion), Msm, Pmp attend?
Curtis Griffy (Lion), Msm, Pmp attended Colorado Technical University, Purdue University, Franklin Central High School, Dale Carnegie, Professional Development Days Pmi- Mn, Professional Development Days Pmi- Mn.
What are some of Curtis Griffy (Lion), Msm, Pmp's interests?
Curtis Griffy (Lion), Msm, Pmp has interest in Children, Risk Management Training, Environment, Snow Skiing, Education, Snowshoeing, Hiking, Camping, People, Real Estate Investing.
What skills is Curtis Griffy (Lion), Msm, Pmp known for?
Curtis Griffy (Lion), Msm, Pmp has skills like Cross Functional Team Leadership, Program Management, Testing, Project Management, Management, Leadership, Pmp, Strategy, Ms Project, Quality Assurance, Medical Devices, Manufacturing.
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