Summary
Overview
Work History
Education
Skills
Timeline
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Brandon Thompson

Cordova

Summary

To work with an organization where delivering excellence in product design, quality, compliance and regulatory are a priority. My background includes 10 years of quality operations, regulatory, compliance, engineering, management, and manufacturing production. During my career, I have worked diligently to ensure my employer provided the best possible product to its customers.

Overview

12
12
years of professional experience

Work History

Lead Auditor

DQS
05.2023 - 09.2023
  • Develops scope of certification and audit agendas through consultation with customer
  • Confirms audit days are adequate based on headcount and complexity
  • Presents audit plans to customer and audit team
  • Determines the customer’s degree of readiness for assessment to appropriate standards
  • Assists customers in understanding the standard and program requirements
  • Directs the conduct of the audit and the activities of audit team members
  • Assesses the conformance of the management system to multiple standards through performing system and process audits
  • Documents audit results including audit trails, strengths and opportunities and nonconformities
  • Prepares audit reports and supporting documentation
  • Reaches team consensus on the audit results having final responsibility for the team conclusions
  • Presents results of audit to client verbally and in writing
  • Assists in analyzing customer responses to nonconformities for acceptance.

Client Manager

BSI
07.2021 - 05.2023
  • Contact clients schedules the visit, plan the assessment, makes appropriate travel plans, conducts assessments, complete reports, and manage results
  • Utilize past experience in engineering, design, or quality control of medical devices, combined with internal BSI training to conduct ISO 13485 audits and CE Marking activities for clients to ensure products meet international standards
  • Delivered BSI third party audit services to assigned clients in accordance with all Schemes and regulatory requirements to assure timely, cost-effective service that assures satisfaction of customer needs
  • Managed multiple clients based on geographic location and a match of qualifications and client contact requirements
  • I’m also responsible for monitoring the client accounts to ensure that records, Point Global information, visit cycle, invoicing and other related matters are properly dealt with to assure client satisfaction is maintained.

Quality Engineer

Titan Medical 758 Bartlett Corporate Dr
10.2018 - 04.2021
  • Participated in new product launches and print reviews where I collaborated with customers to ensure the design was manufacturable to their specified requirements
  • Created macro process maps for efficiency and visual flow of manufacturing processes such as machining, citric passivation, glass bead, inspection, tumbling, welding, and laser marking
  • Created a Detail Process Flow Diagram verification & validation for process inputs and outputs for customer requirements
  • Created control plans for customers to document inspection, Gage R&R Percentage, sampling plan and control methods to ensure the product meets quality standards
  • Coordinated with outsource suppliers on monitoring their risk management activities involving Anodizing, Chrome Coating and Tin coating
  • Devolved PFMEA to manage risk according to critical design features for new product to align with vendors (ISO 14971)
  • Created quality and manufacturing inspection plans by critical design features using calipers, micrometer, height gage and inspection expert software
  • Created overlays for quality and manufacturing to measure profiles using MS Solid Works and vision gauge
  • Executed PQ protocols to ensure the process is capable of manufacturing The Product and to provide documented evidence

Quality Technician

Titan Medical 7580 Bartlett Corporate Dr
08.2017 - 10.2018
  • Performed first check laser mark verification using vision system before full production run
  • Logged inspection results in appropriate format using the quality inspection template
  • Performed final inspection on class I, II, III Medical device Implants
  • Performed first article and first production run studies as required
  • Performed all visual inspection at all stages of manufacturing such as laser marking, chrome coating, Tin coating, and anodize
  • Reviewed routers, inspections, heat certification, material certification documents for acceptability and GMP requirements are met to ISO 13485.

Machinist

E Brooks
06.2011 - 01.2013
  • Performed simple setups and operated Haas CNC to manufacture implants
  • Read and interpreted manufacturing blueprints to the specifications
  • Performed secondary washing for trigen nails to help remove any contamination and oils from the product
  • Establish cuter compensation and tool offsets to improve the tool wear of the drill also, the finished product
  • Performed inspection and gaging using comparator, micrometer, calipers, thread gage & k-gage
  • Performed daily maintenance such as replacing fluids, replacing filters for multiple CNC Machines
  • Performed secondary operation such as glass bead for smoother surface and removable of surface contaminants

Education

Associates Tool & Die Technology -

Northeast Mississippi Community College

B.S - Industrial Engineering Technology

Southern Illinois University

Skills

  • Manufacturing Processes
  • Blue Print Reading
  • Supplier Corrective Action
  • Risk-Management (PFMEA)
  • Conducting 9001 & 13485 ISO Audits
  • Good Manufacturing Practices (GMP's)

Timeline

Lead Auditor

DQS
05.2023 - 09.2023

Client Manager

BSI
07.2021 - 05.2023

Quality Engineer

Titan Medical 758 Bartlett Corporate Dr
10.2018 - 04.2021

Quality Technician

Titan Medical 7580 Bartlett Corporate Dr
08.2017 - 10.2018

Machinist

E Brooks
06.2011 - 01.2013

Associates Tool & Die Technology -

Northeast Mississippi Community College

B.S - Industrial Engineering Technology

Southern Illinois University

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