Coordinate harmonization project in transitioning and re-numbering of controlled documents in Quality System.Analyze the impact of proposed changes by assuring correctness in documentation.Ensure accurate and complete processing of Item Master, BOM structure and RoHS documentation.Revise and route document change requests to support project deliverable with Agile Document Management Software. Conduct Change Control Board Meeting weekly to ensure documents follow the guidelines as outlined in the documentation SOPs and GDPs.Communicate with Change Orders Originators to make necessary correction and additions to the change prior routing the change for approval status.

Analyzed and reported product quality and installation data for HP Server and Storage products. Provided meaningful information on data processes simplification and operational efficiencies.Developed expertise and practical knowledge of applications within business environment. Provided information, analysis and recommendations in support of team efforts.Supported the Quality re-engineering and re-design initiatives by coordinating and compiling statistical analysis in various data related formats, utilizing mathematical modeling tools.

• Provided client with customer data, by relating / mapping customer data from multiple source systems into a central, consolidated company-wide customer database.• Managed customer account for sales support function.• Reported sales group or Cisco internal system through remedy tool.• Handled customer and collaborator requests with attention to speed, detail and respect of the company business rules.• Mapped/related incoming customer data in a timely manner, report company hierarchy issues.• Provided input to improve customer data processing by researching and analyzing the validity of the information received in different languages.• Participated in user acceptance testing for software enhancements.• Assisted other departments with enquiries regarding the customer database.

• Analyzed percentage of alcohol by volume using distillation method.• Conducted qualitative and quantitative testing of alcohol and raw materials.• Ensured that the brand and proof are compliant prior to start of bottling run.• Conducted package quality inspection and quality audits and isolate product that do not meet standards.• Audited container rinsers, air blowers, filters, and coders to ensure proper operations.

• Provided documentation support to all departments in Fremont site, practiced cGMP and GDP.• Responsible for processing, managing and maintaining high volume of alpha and numeric documentation into Access database.• Issued and reconciled Equipment/ Instrument Use Logs, Batch Production Records and Laboratory Notebooks.• Organized the documentation department and prepared for the FDA audit, EMEA audit, and Internal audit.• Reviewed and modified SOPs, work instructions and reports.• Cross-trained team members in archiving and retrieving of completed records to the File Room in Fremont Site using File Trail System.• Retained and archived completed records in accordance with the Amgen Records Retention Schedule.• Performed periodic review and reconciliation of records in the File Room.• Ensured change control requirements have been met and the content is acceptable.

• Conducted qualitative and quantitative testing of beverages, syrups, and raw materials throughout the entire production process. • Analyze syrup beverage and/or water attributes.• Audited container rinsers, air blowers, filters, and coders to ensure proper operations.• Conducted package quality inspection and quality audits and isolate product that do not meet standards. • Received and test carbonation and all raw materials prior to production process.• Practiced GMP and GLP and to maintain highest possible house-keeping standards to prevent microbial contamination.