John Chipman Email and Phone Number
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John Chipman personal email
John Chipman is a Senior Specialist, Quality Assurance at Zoetis Inc. at Zoetis. He possess expertise in validation, gmp, raw materials, supplier quality, lot disposition and 19 more skills.
Zoetis
View- Website:
- zoetis.com
- Employees:
- 7922
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Senior Compliance Specialist Quality OperationsZoetis Mar 2021 - PresentKalamazoo, Michigan, United States
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Quality Assurance SpecialistZoetis Inc. Mar 2015 - Mar 2021Kalamazoo, Michigan AreaInvestigate product quality complaints, interacting with local and international contacts. Support supplier quality through on site audits. Support site regulatory compliance.
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Sr. Associate / Incoming Materials Quality AssuranceZoetis Feb 2014 - Mar 2015Kalamazoo, Michigan AreaResponsible for reviewing and approving incoming raw material materials and secondary packaging materials used in Kalamazoo operations. Perform supplier audits, both regular and 'for cause' audits. Repsonsible for Quality support for warehousing functions. Qualtiy oversite for change control procedures. Secondary responsibilites for site training documentation.
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Sr. Associate / Quality OperationsZoetis Mar 2012 - Jan 2014Kalamazoo, Michigan AreaResposible for lot release, production deviation investigations, annual product reviews, review of documentation for change control purposes. Administration of site change control, and site training documentation platform. QO Incoming Raw Material suppport, qualified Supplier Auditor. Provide support for internal and external regulatory audits.
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Qo Labortory Technician VPfizer, Inc Dec 2008 - Feb 2012, Animal Health Drug ProductPerform routine analysis onfor Animal Health Ddrug products, specifically Ceftiofur products.Perform instrument calibrations and qualification as required.Perform special projects as directed by Laboratory management. -
Chemist, Cleaning Validation Method DevelopmentPfizer, Inc May 2004 - Nov 2008Chemist, Cleaning Validation Method DevelopmentDevelop and validate test assays for use by the Rapid Turn Laboratory to verify the cleanliness of API production equipment.Write and execute cleaning verification protocols and publish the resulting validation reports.Write and implement cleaning verification test assays through the DRA/ECC system for use in the Rapid Turn Lab .Lab.Work closely with API Plant Professionals to maintain current standards in the cleaning validation program. This includesd consultation for and approval of Cleaning Validation Protocols and Cleaning Evaluation Reports.Perform assessments of the impact of new products on established protocols.Perform the cleaning validation monitoring and release of equipment cleaning used in the manufacture of drug product in Building 41.
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Technical Team LeadAnalytical Testing Hplc Laboratories Mar 2002 - May 2004Plan and organize the daily activities in of a fast paced HPLC lab to assure timely release of data to production.Perform laboratory investigations for out of specification results, out of target results, and out of trend data in a timely manner.Investigate DNR trends to determine root causes and long term solutions.Provide input to laboratory management as to personnel issues.Assist laboratory personnel with assay and Diamir/Galaxie issues.Develop plans to update all analytical instrumentation to insure ensure a high degree of reliability in the quality of the unit's results
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Laboratory Professional IiiPfizer, Inc Dec 2000 - Mar 2002
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Quality Control Analyst Iii / Quality Analytical LaboratoryAtrix Laboratories, Inc Aug 1996 - Nov 2000Perform routine analysis of incoming raw materials, in- process and finished products.Assist in new product and technology transfers for Analytical R&D.Investigate and implement analytical method improvements.Perform instrument calibrations and annual qualifications for all HPLC's.
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Gmp Coordinator / Analytical R&DGeneva Pharmaceuticals Mar 1993 - Oct 1995Work with site QA to prepare for and participate in FDA pre-approval inspections.Direct AR&D management response during audits. Coordinate chemist interviews with auditors.Meet with FDA investigators during inspections and respond to their inquiries in a timely manner.Coordinate training/qualification of all Analytical R&D laboratory personnel.Schedule instrument calibrations and for all laboratory equipment in AR&D.Perform investigations of for out of trend as well asand out of specification data.Perform regular audits of the laboratory to insure ensure adherence to cGMP's and company SOP's.Advise and coordinate information for new instrument purchases.
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Chemist / Analytical R&DGeneva Pharmaceuticals Feb 1987 - Mar 1993Develop and validate test assays for raw materials and finished products for products under development.Perform analysis of incoming raw materials, in- process and finished products, in support of product/process development.Provide analytical data for publication as a part of ANDA's (Abbreviated New Drug Applications).Assist in new product and technology transfers from Analytical R&D to Quality Control.Perform instrument calibrations for all HPLC's.
John Chipman Skills
John Chipman Education Details
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Chemistry
Frequently Asked Questions about John Chipman
What company does John Chipman work for?
John Chipman works for Zoetis
What is John Chipman's role at the current company?
John Chipman's current role is Senior Specialist, Quality Assurance at Zoetis Inc..
What is John Chipman's email address?
John Chipman's email address is jo****@****zer.com
What schools did John Chipman attend?
John Chipman attended University Of Northern Colorado.
What skills is John Chipman known for?
John Chipman has skills like Validation, Gmp, Raw Materials, Supplier Quality, Lot Disposition, Change Control, Deviations, Auditing, Asceptic Processing, Qaqc, Tlc, Hplc.
Who are John Chipman's colleagues?
John Chipman's colleagues are Joshua Lawrence, Daniel Perez, Eduardo Muniz, Manuel Verde Bua, Maciej Wasiluk, Sean Spagnoli, Giuseppe Di Fazio.
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