Debra Walton

Debra Walton Email and Phone Number

Retired Quality Assurance & Regulatory Affairs Specialist
Debra Walton's Location
Peculiar, Missouri, United States, United States
Debra Walton's Contact Details

Debra Walton personal email

n/a
About Debra Walton

Debra Walton is a Retired Quality Assurance & Regulatory Affairs Specialist.

Debra Walton's Current Company Details

Retired Quality Assurance & Regulatory Affairs Specialist
Debra Walton Work Experience Details
  • Elanco
    Regulatory Affairs Specialist
    Elanco Aug 2020 - Dec 2021
    Shawnee, Kansas, United States
    View
  • Bayer Animal Health
    Regulatory Affairs Specialist
    Bayer Animal Health Mar 2019 - Jul 2020
    Shawnee County, Kansas, United States
    View
  • Bayer Animal Health
    Continued Process Verification Specialist
    Bayer Animal Health Feb 2016 - Feb 2019
    Shawnee, Ks
    View
  • Propharma Group
    Qa Consultant
    Propharma Group Jan 2014 - Jan 2016
    Overland Park, Ks
    View
  • Carefusion
    Sr Specialist, Regulatory Affairs
    Carefusion Jan 2011 - Nov 2013
    Leawood, Ks
    Maintained the new drug applications (NDA) for human OTC drug products. Worked with manufacturing site personnel on supplement strategies and submission preparation for CMC changes. Coordinated and compiled the annual reports for each NDA. Created and submitted the electronic drug listings, establishment registrations and labeler code requests for all products. Worked with marketing and legal teams on product literature development to assure these materials met FDA regulations.
    View
  • Propharma Group
    Qa Associate
    Propharma Group 2008 - 2010
    Overland Park, Ks
    Contracted to CareFusion's Regulatory Affairs department in Leawood, KS to assist with routine FDA reporting.
    View
  • Aptuit
    Director Quality Systems
    Aptuit 2007 - 2008
    Kansas City, Mo
    Leader of the quality systems group responsible for CAPA, supplier audits, computer system validation, and standard operating procedure administration. Co-leader of a team of consultants responsible for developing and initiating GMP remediation and regulatory body inspection preparedness activities at the site.
    View
  • Pfizer
    Qa Manager
    Pfizer 2000 - 2007
    Lee'S Summit, Mo
    Leader of the quality assurance department at animal heath manufacturing plant. This department was responsible for raw material release, finished product release, environmental monitoring, deviation investigations, change management, supplier auditing and labeling. Products included sterile injectable, topical, and feed supplement dosage forms that were distributed globally.
    View

Debra Walton Skills

Gmp Fda Capa Regulatory Affairs Quality System Quality Auditing Validation Change Control 21 Cfr Part 11 Quality Assurance Sop Computer System Validation Gxp V&v Regulatory Requirements U.s. Food And Drug Administration Standard Operating Procedure Corrective And Preventive Action Cgmp Regulatory Reporting

Debra Walton Education Details

Frequently Asked Questions about Debra Walton

What is Debra Walton's role at the current company?

Debra Walton's current role is Retired Quality Assurance & Regulatory Affairs Specialist.

What is Debra Walton's email address?

Debra Walton's email address is de****@****nco.com

What schools did Debra Walton attend?

Debra Walton attended Missouri State University.

What skills is Debra Walton known for?

Debra Walton has skills like Gmp, Fda, Capa, Regulatory Affairs, Quality System, Quality Auditing, Validation, Change Control, 21 Cfr Part 11, Quality Assurance, Sop, Computer System Validation.

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