Quality Control A Team

LARRY H SEGURA

*****.*****.**@*****.*** 801-***-****

PROFILE

I have been working in the quality control field for fourteen plus years. I’m looking to work with a great company that I can grow and share my knowledge and experience with. I am highly motivated Organized, dedicated and ambitious professional with excellent attention to detail. A team player who works well with others to achieve a positive work environment. I Also have experience communicating with all different personalities over the phone, email, and in person. I am quick to adapt to change while balance attention to detail and task prioritization.

May 2023

Present

February 2022-

April 2023

September 2019-Feb 2022

LACO Technologies

Perform Incoming inspections.

Inspect all Custom parts.

Perform all tools Calibration.

Scanning all document in to system.

Perform all in process inspections.

Perform all final inspections.

Sleep Number

• Perform audits in receiving, manufacturing, assembly, final and fulfillment functions, as required.

•Report non-conformances discovered during work activities and consult with area leaders to take appropriate action to prevent further processing and/or recurrence.

•Verify discrepant materials and product, make use of the Discrepant Material Report (DMR) database where applicable.

•Accurately input data in database and publish reports.

•Assure inspection/audit files contain current engineering drawing revisions and current manufacturing procedures for the functional area.

•Assist in developing corrective and preventive actions to eliminate nonconformance.

•Support development of the Sleep Number quality system.

•Support compliance with the Federal Flame-Retardant Standards including ensuring that burn test beds are built and documented correctly, as required.

•Recommend Quality bulletins determined from audit findings and or assist in One Point Lesson training articles.

•Communication of non-conformances as required to the supplier.

•Follow all Company documented procedures including safety work instructions etc.

•Participate in continuous improvement initiatives.

•Other duties as assigned by management.

Flexan, LLC SLC UT, Quality Control Inspector

•Read blueprints and specifications

••Performed visual, dimensional, and functional inspection of components and/or finished medical device products using a wide variety of tools and equipment such as magnifying lamp, microscope, vision inspection system, etc. to ensure conformance with design specifications; utilize a microscope in the inspection of equipment, in keeping with associated SOP; may also operate automated inspection equipment to verify dimensional requirements

•Reports quality issues and discrepancies to the QC Supervisor/QC Supervisor – Probiotics

July 2018 -May 2019

July 2016- May 2018

November 2014- July 2016

SKF USA Industrial Seals W, V, C UT, Quality Control Inspector

•Conducted visual and measurement tests based on existing working instructions and standards for raw materials and packaging materials.

•Monitors and verifies production processes and outgoing products.

•Reports quality issues and discrepancies to the QC Supervisor/QC Supervisor – Probiotics

•Follows up on quality decisions to ensure corrective actions will take/have taken place on, but not limited to: questionable products on hold; rejecting non-conforming materials to the supplier; non-conforming products for re-processing.

•Collects and organizes sample(s) of raw materials/semi-manufactured products/finished goods for laboratory tests and further reference.

•Performs inspections following our GMP, HACCP or any other quality system in place (E.G.: Personal hygiene, Cleaning, Pest control, Transportation, Storage).

•Performs temporary assignments as needed.

Edwards Lifesciences S, L, C UT, Quality Associate

•Performed visual, dimensional, and functional inspection of components and/or finished medical device products using a wide variety of tools and equipment such as magnifying lamp, microscope, vision inspection system, etc. to ensure conformance with design specifications; utilize a microscope in the inspection of equipment, in keeping with associated SOP; may also operate automated inspection equipment to verify dimensional requirements

•Perform functional testing of finished medical device products using both automated and manual valve testing equipment to ensure conformance with design specifications

•Conduct operational audits and documentation reviews to ensure compliance with applicable procedures and documentation standards

•Review, follow and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records and utilize a variety of computer programs to perform and/or document specific job tasks

•Provide constructive team feedback, including escalating work issues and changes in the final devices to supervisor for assessment and correction

•Perform line clearance and verification of inspection

•Perform verification of manufacturing documents with component and device drawings

Integra life Sciences Corporation S L C, UT, Quality Associate

Provided Plant Quality compliance support for the following Quality tasks and duties: Maintain site Corrective and Preventive Action, Non-conforming Materials and Complaint programs. Perform Final Inspections including Final Product Release. Certify to internal auditor requirements and conduct internal audits as necessary. Provide back-up in other QA areas where necessary, including In-Process Inspections, Load Releases to Sterilizer, Label Reviews, and Device Master Records etc. Assist in the introduction of new or improved processes. Act as a member of problem-solving teams. Facilitate and assist the development, implementation and monitoring of quality programs and policies that ensure that the development, manufacture and distribution of medical products in compliance with corporate policies, U.S. Food and Drug Administration regulations, ISO 9001, ISO 13485:2003, the Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other

EDUCATION

(Threat Assessment Group) (TAG) Work place Violence Prevention Trainer Graduated: 3/2007 S, L, C, UT Cert instructor (Community Emergency Response Team) S, L, C Fire Dept.

FEMA certified Graduated: 7/2004 S, L, C, UT ERT Train the Trainer (Emergency Response Team) Enviro Safetech Inc.

Custom Parts Inspection

KEY SKILLS AND CHARACTERISTICS

•Business Math

• Microsoft Office Suite

•Internet navigation

•Male/ Female Taper

•Calipers

•Ring Gage

•Steel rulers

Burst test

Calibration

•Laser or Optical Micrometer

•Adaptability

•MSMD

•Nikon system

•Chatillon Universal Tester

•Leak testing

•Tensile testing

Borescope system

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