Sabrina Whitt

Sabrina Whitt Email and Phone Number

Senior Global Product Quality @ Eastman Chemical Company
Sabrina Whitt's Location
Johnson City, Tennessee, United States, United States
Sabrina Whitt's Contact Details

Sabrina Whitt personal email

n/a
About Sabrina Whitt

Sabrina Whitt is a Senior Global Product Quality at Eastman Chemical Company. She possess expertise in change control, gmp, quality assurance, validation, pharmaceutical industry and 45 more skills.

Sabrina Whitt's Current Company Details
Eastman Chemical Company

Eastman Chemical Company

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Senior Global Product Quality
Sabrina Whitt Work Experience Details
  • Eastman Chemical Company
    Senior Global Product Quality
    Eastman Chemical Company Nov 2017 - Present
    Kingsport, Tennessee, Us
    Accomplish bottom-line results by managing numerous global product lines such as visual material plastics and pharmaceutical excipients. Develop change controls, complaints, investigations, protocols, and standard operating procedures. Carry out internal and vendor audits. Hold full accountability for approving CAPAs, master batch records, and receiving paperwork. Liaise with multiple regulatory agencies and client inspections. Organize several meetings regarding quality at Kingsport sites. Examine calibrations, procedures, and reports. Serve as quality SAP representative. Generate certificates of analysis for products.
  • Pure Foods Inc
    Director Qa
    Pure Foods Inc Mar 2015 - Nov 2017
    Achieved shared vision and objectives by directing one documentation specialist, three quality supervisors, and numerous lab technicians in four locations. Led departmental activities including include hiring, training, performance evaluation, and developing all department employees. Delivered advanced technical assistance to key members in maintaining Sage ERP system. Operated PCR lab for non-GMO specialized testing as well as carried out item and supplier set-up and approval and vendor audits. Coordinated meetings associated with quality within Kingsport and two Bristol sites. Generated certificates of analysis for all products. Conducted GMP and HR training for all employees. Worked as liaison for multiple regulatory agencies and client inspections.● Attained BRC Level A certification for all 3 sites in the first year of operation.● Implemented PCR lab for non-GMO testing of incoming raw materials.
  • Upm Pharmaceuticals, Inc.
    Senior Qa Manager
    Upm Pharmaceuticals, Inc. Oct 2012 - Mar 2015
    Bristol, Tn, Us
    Attained desired outcomes by spearheading MQA specialists/inspectors and one manager/supervisor. Followed quality metrics on-site. Worked as quality approver to examine stability forms, complaints, change controls, standard operating procedures, master batch records, annual product reviews, and validation documents. Acted as quality lead for SAP system. Served as member of divesture/decommissioning teams. ● Rolled-out corporate change control system. ● Worked as quality expert for three new successful product launches.● Spearheaded execution of batch record review and investigation procedures.
  • Pfizer Pharmaceuticals, Inc. ......    ...  ..      ....
    Supervisor Quality Assurance
    Pfizer Pharmaceuticals, Inc. ...... ... .. .... May 2011 - Oct 2012
    Supervises quality assurance manufacturing and packaging inspectors. Coordinates with multiple departments on all cGMP changes. Conducts weekly Change Control meeting . Audits completed batch records and incoming components. Investigates product complaints. Participates on multiple product teams. Involved in making reports. Input statistical data on PC. Reviews all internal procedures. Write and edit procedures. *... Coordinates with multiple departments all cGMP changes*... Conducts weekly Change Control meeting*... Supervises quality assurance manufacturing and packaging inspectors
  • Pfizer/King Pharmaceuticals, Inc.
    Change Control Project Manager - Quality Assurance
    Pfizer/King Pharmaceuticals, Inc. Nov 2007 - May 2011
    Coordinates with multiple departments on all cGMP changes. Conducts weekly Change Control meeting . Audits completed batch records. Investigates product complaints. Participates on multiple product teams. Involved in making reports. Input statistical data on PC. Reviews all internal procedures. Write and edit procedures. *... Coordinates with multiple departments all cGMP changes*... Conducts weekly Change Control meeting*... Featured Speaker for the Institute of Validation Technology's 9th Annual Change Control Conference
  • King Pharmaceuticals, Inc. ......    ...  ..      ....
    Laboratory Chemistry Technician I - Quality Control
    King Pharmaceuticals, Inc. ...... ... .. .... Nov 2003 - Nov 2007
    Audits completed stability and micro-biology reports. Part of validation team for eInfotree software. Responsible for supply orders. Reconciles budget. Involved in making reports. Input statistical data on PC. Performs analysis of statistical information. Write and edit procedures. *... Audit reports, calibrations, and procedures* Input data in SAP system * Create and revise eInfotree templates
  • Virginia Highlands Community College ..........
    Operations Assistant To The Director
    Virginia Highlands Community College .......... Nov 2002 - Aug 2003
    Center of Business and Industry Responsible for book and supply orders. Coordinates, with faculty, the class schedule for all credit bearing classes under CBI. Responsible for creating and distributing news releases. Involved in making faculty reports. Input statistical data on PC.*...Communicate with faculty on a daily basis to determine future plans and needs. *...Resolve scheduling problems in a meticulous and organized fashion.
  • Virginia Highlands Community College ............
    Mathematics Instructor And Student Advisor
    Virginia Highlands Community College ............ Aug 1999 - Aug 2003
    Instruct students in Algebra I, Algebra II, Basic Mathematics, and Business Mathematics. Responsible for coordinating and facilitating tutoring sessions with students. Provide accurate and timely reports on progress. Student advisor. Facilitate computer tutorials. Developed calculator course for various math applications.*...Communicate with students on a daily basis to ensure their needs and goals are being met. *...Resolve student problems in a meticulous and organized fashion.

Sabrina Whitt Skills

Change Control Gmp Quality Assurance Validation Pharmaceutical Industry Quality System Quality Control Capa 21 Cfr Part 11 Fda Sop Sap Quality Management Quality Auditing Software Documentation Microsoft Excel Lims V&v Contract Manufacturing Statistics Microsoft Office Change Management Computer System Validation Cleaning Validation Gxp Technology Transfer Regulatory Affairs Glp Manufacturing Problem Solving Gamp Regulatory Submissions Hplc Analytical Chemistry Aseptic Processing Gcp Biopharmaceuticals Medical Devices Root Cause Analysis Cgmp Excel Documentation Cross Functional Team Leadership Chromatography Fda Gmp Gas Chromatography Good Laboratory Practice Laboratory Clinical Trials Pharmacovigilance

Sabrina Whitt Education Details

  • King University
    King University
    Business Administration.....
  • Emory & Henry University
    Emory & Henry University
    Mathematics/Education
  • Southwest Virginia Community College.     ...................
    Southwest Virginia Community College. ...................
    Mathematics

Frequently Asked Questions about Sabrina Whitt

What company does Sabrina Whitt work for?

Sabrina Whitt works for Eastman Chemical Company

What is Sabrina Whitt's role at the current company?

Sabrina Whitt's current role is Senior Global Product Quality.

What is Sabrina Whitt's email address?

Sabrina Whitt's email address is sa****@****ter.net

What schools did Sabrina Whitt attend?

Sabrina Whitt attended King University, Emory & Henry University, Southwest Virginia Community College. ....................

What skills is Sabrina Whitt known for?

Sabrina Whitt has skills like Change Control, Gmp, Quality Assurance, Validation, Pharmaceutical Industry, Quality System, Quality Control, Capa, 21 Cfr Part 11, Fda, Sop, Sap.

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