Experience

OrthAlign, Inc.

• United States
• Medical Equipment Manufacturing
• 1 - 100 Employee

• QA Manager

  • Jan 2009 - Present



Orqis Medical

• Medical Equipment Manufacturing
• 1 - 100 Employee

• QA Specialist

  • Jan 2008 - Dec 2008

• Consultant - Quality Assurance

  • 2008 - 2008



JPMorgan Chase & Co.

• United States
• Financial Services
• 700 & Above Employee

• Content Manager

  • Feb 2000 - Jun 2007

  Oversaw department’s daily online publishing requirements. Served as liaison with business partners to address various communication requests.  Created Tracking System for online documentation resulting in improved efficiency.  Established and wrote procedures and service level agreements for online manual updates. Ensured compliance with all internal operating procedures to comply with Federal and State regulations, resulting in clean audits with no findings.  Researched archives for audit requests.  Ensured all published policy communications were incorporated into online manuals.  Awarded “2004 Summit Club” honors for overall performance excellence. Show less

• Web Content Manager

  • 2000 - 2007



Washington Mutual

• Content Manager

  • 2000 - 2007



Sorin Biomedical

• Technical Writer

  • Apr 1989 - Dec 1999

  Sorin Biomedical was a manufacturer of cardiovascular medical devices.  Wrote instructions for use of software and conducted employee training that resulted in improved productivity and efficiency.  Researched and wrote manufacturing and standard operating procedures.  Maintained Device Master Records and Device History Records.  Key team member for the production of training sessions and training videos focusing on correct documentation practices and Good Manufacturing Practices for company-wide use. Show less



Sorin Group

• Document Control

  • 1989 - 1999



Home Savings Bank

• United States
• Banking
• 200 - 300 Employee

• Policy and Procedure Analyst

  • Sep 1987 - Apr 1989



Bentley Laboratories -Division of Baxter Travenol

• Documentation System Analyst

  • May 1980 - Jul 1987

   Wrote policies and procedures.  Coordinated the creation of Device Master Record files for all products to ensure compliance to FDA regulations.  Produced off-site GMP training sessions for the Certification of Quality Assurance employees.  Wrote policies and procedures.  Coordinated the creation of Device Master Record files for all products to ensure compliance to FDA regulations.  Produced off-site GMP training sessions for the Certification of Quality Assurance employees.