Partnered with Engineering to build and execute a PQ program designed to qualify seven new/rebuilt packaging lines over the course of three months.Process Mapped several key workstreams related to packaging processes. Identified gaps, worked with cross functional teams to implement strategies for resolution.Developing a program for identification of Challenging Bulks as they relate to packaging efficiencies (OEE).Designed/Executed Stability Packaging Trials.

o Formulate nutritional supplement products in tablet, capsule and softgel forms in support of manufacturingo Assists with creating and approving new raw material specifications, master batch records, change controls, deviations or other required documentation in support of manufacturing existing in-line productso Assists in scale up, validating and transferring technologies/processes to other internal manufacturing sites, or externally o Provides technical support to manufacturing including but not limited to formulation or process improvement, formulation globalization, cost savings initiatives, and trouble shootingo Interacts with multi functional teams (including Quality, Procurement, Product Development and Manufacturing) to resolve issues as may arise in the course of new product development or existing product improvemento Negotiates timeline commitments among other team members such that agreed objectives and timings for completion of activities are achieved

Maintains control of all electronic and non-electronic documents, as well as administers the Change Control and product cost quoting systems as they relate to R&D functionsEnsures proper formatting is followed for the various R&D documentsMaintains the filing of current and archived Master Batch Records Assists in the ordering of office supplies for the departmentProject management of the approvals of change control requests in PLM and Master Batch Record approvals as it relates to Research and Development Data entry of new formula and revisions to Master Batch Records under the direction of the R&D Scientist or R&D Assistant Scientist utilizing customized SQL applications.Interacts with Quality Assurance, Quality Control, Procurement, Manufacturing and Nutrition Department to ensure the distribution of revised and needed documents in a timely mannerPerforms special projects as are assigned by the R&D Document Manager/R&D Manager or R&D Director.

Duties below are in addition to specified duties listed as QC Lab Coordinator Purchaser of supplies for the Microbiology lab Maintenance of procurement-card purchases & reports.Coordination of projects Send samples out for testingGenerate and maintain spreadsheets if applicable. Follow up as necessary.Liase with IT for EMC's InputAccel and Application Xtender (document retention software)Coordination and participation in meetings and conference calls to determine business requirementsCreation of Project Definition DocumentWork directly with IT and VendorCreation of training documentsTravel to external sites for deployment and trainingAdministration of software on an "as needed" basis

Provide requested documentation throughout the company in a timely mannerAccurately record data utilizing Microsoft Excel and various custom written Lotus Notes databases.Creation of reports and statistical information on an as-needed basis when requested by management.Coordination of documentation throughout the company. Process harmonization throughout the company in preparation for upcoming changes in FDA industry regulationsCreation of specification forms for in-house product testing.

Lead Associate in the review of vendor packaged goods.Coordinate and meet with product development and purchasing departments to discuss quality issues of the products.Investigate customer complaints to determine validity and fault. Communicate results.Travel to off site locations to sample additional product to be tested as requested by management.Speak directly to vendors to obtain missing paperwork and discuss how to assure the best quality for our products.Creation of product specification forms for vendor packaged goods.