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Ina E Hammond, 471063 Gianna Ave, Fort Lupton, CO 80621

Ina Hammond Phones & Addresses

Broomfield, CO   

McHenry, IL   

Oceanside, CA   

Canyon Country, CA   

Jonesboro, GA   

Glenarden, MD   

Pikesville, MD   

Newbury Park, CA   

Saint Louis, MO   

Claremont, CA   

4765 Frazee Rd APT 1423, Oceanside, CA 92057   

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Ina E Hammond

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Work

Company: Avexis, inc. Jun 2017 Position: Principal engineer

Education

Degree: Bachelors, Bachelor of Science School / High School: California National University For Advanced Studies 2008 to 2011 Specialities: Management, Engineering

Skills

Validation • Gmp • Change Control • Fda • Cleaning Validation • Biopharmaceuticals • V&V • Pharmaceutical Industry • Sop • Biotechnology • Quality Assurance • Quality Control • Capa • 21 Cfr Part 11 • Computer System Validation • Glp • Aseptic Processing • Trackwise • Cip • Lims • Process Validation • Commisioning • Gamp • Equipment Validation • Temperature Mapping • Performance Qualification • Facilities Management • Facilities Qualification • Solid Dosage Pharmaceuticals

Industries

Biotechnology

Mentions for Ina E Hammond

Ina Hammond resumes & CV records

Resumes

Ina Hammond Photo 9

Principal Engineer

Location:
1893 Brush Oak Ct, Newbury Park, CA 91320
Industry:
Biotechnology
Work:
Avexis, Inc.
Principal Engineer
Genentech Sep 2013 - Jun 2017
Validation Engineer
Dendreon Sep 2010 - Jan 2012
Validation Engineer Ii
Validation Technologies, Inc. Nov 2008 - Sep 2010
Senior Validation Specialist
Shire May 2008 - Oct 2008
Qa Validation Associate Ii
Validation Technologies, Inc. Jan 2007 - Apr 2008
Engineering and Validation Specialist
Kv Pharmaceutical Dec 2003 - Jan 2007
Validation Specialist
Kv Pharmaceutical Oct 2002 - Dec 2003
Validation Technican
Education:
California National University For Advanced Studies 2008 - 2011
Bachelors, Bachelor of Science, Management, Engineering
Skills:
Validation, Gmp, Change Control, Fda, Cleaning Validation, Biopharmaceuticals, V&V, Pharmaceutical Industry, Sop, Biotechnology, Quality Assurance, Quality Control, Capa, 21 Cfr Part 11, Computer System Validation, Glp, Aseptic Processing, Trackwise, Cip, Lims, Process Validation, Commisioning, Gamp, Equipment Validation, Temperature Mapping, Performance Qualification, Facilities Management, Facilities Qualification, Solid Dosage Pharmaceuticals

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