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Shannon Stone
1016 Grant Street
Phone: 641-969-3528
Mobile: 641-814-3128
E-mail: shannon_stone@cargill.com
Objectives
Experienced FSQR Specialist with 16 years Quality Management experience seeking new challenges and
opportunities for development..
Experience
FSQR Quality Management Specialist/Supervisor (Lead Associate)(06/2004 –Present)
Cargill (Eddyville, IA USA
 Manage supplier/vendor evaluation (SEM) & approval systems that encompasses raw materials,
packaging materials, processing aids/ingredients, transportation, warehouses, etc.
 Manage SEM audits for current and potential external manufacturers.
 Participate in or independently conduct both internal and external audits at potential and current
suppliers, co-manufacturers, warehouses, transportation facilities, storage facilities, etc.
 Create and maintain Quality Management procedures and policies to ensure compliance to
government regulations and customer requirements.
 Perform QM activities that include: managing Master Manufacturing Records, Batch Record
systems, review and release of finished products produced in Eddyville and at co-manufacturers
for the Sterol Derivatives product lines.
 Review and approve all Management of Change (MOC's) for Eddyville including procedural
creation/revisions, equipment optimization or changes, processing changes, material changes, etc.
 Serve as a liaison between Operations and GMP/regulatory compliance.
 Manage activities involving HACCP, GMP's and food safety initiatives cross-functionally in
Eddyville and with other product lines as needed. Review customer contracts including
requirements for GMP compliance, product specifications, shipping requirements, packaging
requirements, etc.
 Collaborate with Product Line Managers, Customer Service, Sales Team, Operations, and Supply
Chain to ensure Cargill's protected.
 Manage Quality Assurance Administrative Assistant.
 Comply with all government regulations and Cargill policies and procedures which include but
are not limited to environmental, safety, HACCP, and cGMP.
 Develop and maintain internal auditing/verification protocols. This includes collaborating with
Supply Chain and Procurement teams in Eddyville, CHN, and Cargill Corporate.
 Lead customer and compliance audits for Eddyville and Sterol Derivatives.
 Create and implement IDOCs document management system for CHN BU.
 Manage Document Control Systems in the continuous optimization of the QM department,
including the development, maintenance, and review of Standard Operating Procedures.
 Train new employees and contractors in areas of HACCP, Food Safety, and GMP's. Also provide
annual training to all employees.
 Resume: Shannon Stone
 Page 2
PLTP QM Super user Tester TEMPORARY ROLE (01/2010 –01/2012)
Cargill (Eddyville, IA USA
 Provided solutions for requirements that did not fit in SAP.
 Provided information on legacy systems for comparison to SAP.
 Provided input for creation of materials.
 Entered data for specifications, inspection plans, master inspection characteristics, and methods.
 Approval to customer vendor lead for adding new vendors in SAP.
 Approval to material master lead for reviewing new materials for adding to SAP.
QA Administrative Assistant (05/2000 –05/2004)
Cargill (Eddyville, IA USA
 Responsible for managing samples sent to contract laboratories including managing data, pricing,
time of completion, and reporting to information to management and appropriate personnel.
 Responsible for receipt, review, and release of all bulk and non-bulk raw materials, ingredients,
and processing aids for Eddyville.
 Responsible for QA record maintenance including: issuing, collecting, controlling, collating, filing,
and archiving.
 Responsible for providing QA assistance in training, auditing, and documentation. Also provide
back-up coverage for QA Supervisor as needed.
 Perform miscellaneous job-related duties as assigned (scanning documents, word docs, creating
and entering data into spreadsheets, provide back-up for Executive Secretary.
Education
Computer Programming (1998 – 2000)
Indian Hills Community College in Ottumwa IA.
Skills
Strengths
 Qualified SEM Auditor.
 External Manufacturing and Supplier auditor experience since 2003.
 Managing internal and external customer relationships.
 Archer Experience, enter audit data into Archer.
 SAP Implementation and live experience.
 Verbal and written communication skills.
 Managing conflict regarding enforcing requirements.
 Great attention to detail.
 Contacts within Supply Chain Sourcing, Procurement, Sales, and Customer Service.
 Document Management experience: Creation, review, approval, and revision of standard
operating procedures for Eddyville and CHN/CCMNA BU.
 Strong computer skills including but not limited to Microsoft Excel, Word, and PowerPoint.
 Keen sense of managing priorities and meeting deadlines.
 Ability to work under stress
 Experience with FSSC 22000:2005 ISO/TS 22002-1:2009 and additional FSSC 22000 requirements
 Experience with ICH Q7 for Active Pharmaceutical Ingredients in Europe (GMPs)
 Experience with Dietary Supplement GMPs (21 CFR Part 111)
 Experience with Food GMPs (21 CFR Part 110)

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Shannon Stone 2014 Final

  • 1. Shannon Stone 1016 Grant Street Phone: 641-969-3528 Mobile: 641-814-3128 E-mail: shannon_stone@cargill.com Objectives Experienced FSQR Specialist with 16 years Quality Management experience seeking new challenges and opportunities for development.. Experience FSQR Quality Management Specialist/Supervisor (Lead Associate)(06/2004 –Present) Cargill (Eddyville, IA USA  Manage supplier/vendor evaluation (SEM) & approval systems that encompasses raw materials, packaging materials, processing aids/ingredients, transportation, warehouses, etc.  Manage SEM audits for current and potential external manufacturers.  Participate in or independently conduct both internal and external audits at potential and current suppliers, co-manufacturers, warehouses, transportation facilities, storage facilities, etc.  Create and maintain Quality Management procedures and policies to ensure compliance to government regulations and customer requirements.  Perform QM activities that include: managing Master Manufacturing Records, Batch Record systems, review and release of finished products produced in Eddyville and at co-manufacturers for the Sterol Derivatives product lines.  Review and approve all Management of Change (MOC's) for Eddyville including procedural creation/revisions, equipment optimization or changes, processing changes, material changes, etc.  Serve as a liaison between Operations and GMP/regulatory compliance.  Manage activities involving HACCP, GMP's and food safety initiatives cross-functionally in Eddyville and with other product lines as needed. Review customer contracts including requirements for GMP compliance, product specifications, shipping requirements, packaging requirements, etc.  Collaborate with Product Line Managers, Customer Service, Sales Team, Operations, and Supply Chain to ensure Cargill's protected.  Manage Quality Assurance Administrative Assistant.  Comply with all government regulations and Cargill policies and procedures which include but are not limited to environmental, safety, HACCP, and cGMP.  Develop and maintain internal auditing/verification protocols. This includes collaborating with Supply Chain and Procurement teams in Eddyville, CHN, and Cargill Corporate.  Lead customer and compliance audits for Eddyville and Sterol Derivatives.  Create and implement IDOCs document management system for CHN BU.  Manage Document Control Systems in the continuous optimization of the QM department, including the development, maintenance, and review of Standard Operating Procedures.  Train new employees and contractors in areas of HACCP, Food Safety, and GMP's. Also provide annual training to all employees.
  • 2.  Resume: Shannon Stone  Page 2 PLTP QM Super user Tester TEMPORARY ROLE (01/2010 –01/2012) Cargill (Eddyville, IA USA  Provided solutions for requirements that did not fit in SAP.  Provided information on legacy systems for comparison to SAP.  Provided input for creation of materials.  Entered data for specifications, inspection plans, master inspection characteristics, and methods.  Approval to customer vendor lead for adding new vendors in SAP.  Approval to material master lead for reviewing new materials for adding to SAP. QA Administrative Assistant (05/2000 –05/2004) Cargill (Eddyville, IA USA  Responsible for managing samples sent to contract laboratories including managing data, pricing, time of completion, and reporting to information to management and appropriate personnel.  Responsible for receipt, review, and release of all bulk and non-bulk raw materials, ingredients, and processing aids for Eddyville.  Responsible for QA record maintenance including: issuing, collecting, controlling, collating, filing, and archiving.  Responsible for providing QA assistance in training, auditing, and documentation. Also provide back-up coverage for QA Supervisor as needed.  Perform miscellaneous job-related duties as assigned (scanning documents, word docs, creating and entering data into spreadsheets, provide back-up for Executive Secretary. Education Computer Programming (1998 – 2000) Indian Hills Community College in Ottumwa IA. Skills Strengths  Qualified SEM Auditor.  External Manufacturing and Supplier auditor experience since 2003.  Managing internal and external customer relationships.  Archer Experience, enter audit data into Archer.  SAP Implementation and live experience.  Verbal and written communication skills.  Managing conflict regarding enforcing requirements.  Great attention to detail.  Contacts within Supply Chain Sourcing, Procurement, Sales, and Customer Service.  Document Management experience: Creation, review, approval, and revision of standard operating procedures for Eddyville and CHN/CCMNA BU.  Strong computer skills including but not limited to Microsoft Excel, Word, and PowerPoint.  Keen sense of managing priorities and meeting deadlines.  Ability to work under stress  Experience with FSSC 22000:2005 ISO/TS 22002-1:2009 and additional FSSC 22000 requirements  Experience with ICH Q7 for Active Pharmaceutical Ingredients in Europe (GMPs)  Experience with Dietary Supplement GMPs (21 CFR Part 111)  Experience with Food GMPs (21 CFR Part 110)