Steve Durand Email & Phone Number

Greater San Diego Area

As Sr Application Administrator for Agile PLM my job objective is to define, develop, maintain, and support users for the Agile PLM system. This includes development, design, analysis, evaluation, testing, debugging and implementation of the system in support of cross functional enterprise areas. I also develop and implement policies and procedures to ensure that the system supports the organization's business requirements and meet the needs of the end users.

Irvine, Ca

Responsible for the overall design of Agile PLM based on business requirements. Working as a team member with Project Managers, Developers and Technical business resources to deliver a complete solution for internal business customers. Latest requirements include implementation of UDI solution for class II medical devices per FDA requirements within Agile PLM.

Murrieta, California

Configuration of Oracle/Agile PLM for various clients within the medical device industry. This includes implementation of the Inspirage UDI Solution for FDA compliance.

Irvine, Ca

Responsible for various Agile activities to help bring the system up to its full potential for use at RED. Training employees in the use of Agile both in the Java and Web Client. Responsible for writing processes and procedures as they relate to Agile. Lead on Agile 9.3.2 and EC upgrade to be used in conjunction with ProE. Maintain the Agile system to keep it current with company business requirements.

Ranco Bernardo, Ca

Responsibilities included chairing four separate CCB meetings per week as well as deliverables planning meetings with the purchasing group. Worked with outside vendors to ensure that they had the access that they needed within our Agile documentation system. Other duties included working with internal customers to make sure that they were properly trained in the use of Agile as well as our company documentation procedures.

Poway, Ca

Responsible for assisting in implementing and maintaining the Quality System in compliance with the FDA Quality System Regulation (QSR) and applicable ISO certifications. Primary responsibilities included defining and implementing procedures to support the Quality System, facilitating process validations, supplier evaluation and qualification, internal auditing, MRB, NCMR disposition, facilitating internal quality resolution, maintenance of the corrective and preventive action system and document control/CCB functions.

Irvine, Ca

Responsible for the mechanical design and development of amplifiers for the PCS and cellular industry, requiring a thorough knowledge of extrusions, castings, sheet metal and machining practices. All drawings were done in SolidWorks 2003 or AutoCad 2000 format. Worked on the team that implemented Agile as the company’s documentation management tool. As a manufacturing engineer I was responsible for writing various procedures and design of tools that were required to keep the production lines running efficiently.

Irvine, Ca

Resposible for the mechanical design and documentation of all HUB systems manufactured. Other duties included design and layout of new systems, maintaining existing customer sites as needed, and maintained the engineering documentation using AutoEDMS.