Laura B Kalegaric, Age 544 Smith St, Newbury, MA 01951

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Laura Kalegaric Phones & Addresses

Newbury, MA

17 Worcester St APT 9, Boston, MA 02118 (857) 233-4480

South Dennis, MA

Waltham, MA

Raleigh, NC

Garner, NC

Weston, CT

Social networks

Laura B Kalegaric

Work

Company: Blueprint medicines Aug 2019 Position: Associate director, gmp quality assurance

Education

Degree: Bachelors School / High School: University of North Carolina Wilmington Specialities: Biology

Skills

Supply Chain Management • Validation • Quality System • 21 Cfr Part 11 • Capa • Change Control • Fda • Gxp • Gmp • Lims • Computer System Validation • Glp • Sop • Biotechnology • V&V • Trackwise • Quality Agreements • 21 Cfr Parts 210 and 211 • Biopharmaceuticals • Good Laboratory Practice • Purification • Quality Assurance • Standard Operating Procedure • U.s. Food and Drug Administration • Corrective and Preventive Action

Industries

Biotechnology

Mentions for Laura B Kalegaric

Laura Kalegaric resumes & CV records

Resumes

Associate Director, Gmp Quality Assurance

Location:

Boston, MA

Industry:

Biotechnology

Work:

Blueprint Medicines
Associate Director, Gmp Quality Assurance Nightstar Therapeutics Jul 2018 - Aug 2019
Associate Director, Gmp Quality Assurance Akebia Therapeutics Jun 2017 - Jul 2018
Associate Director, Quality Assurance Akebia Therapeutics Apr 2016 - Jun 2017
Qa Manager, Gmp Alnylam Pharmaceuticals Feb 2015 - Mar 2016
Senior Manager, Qa Supply Chain Momenta Pharmaceuticals Jan 2014 - Jan 2015
Senior Manager Quality Assurance Momenta Pharmaceuticals Mar 2011 - Dec 2013
Manager, Quality Assurance Pfizer Jun 2009 - Mar 2011
Manager, Qa Compliance Pfizer Oct 2003 - Jun 2009
Qa Specialist Iv Serentec 2001 - 2002
Validation Associate Xanthon 2000 - 2001
Technical Services Representative Bayer 1997 - 1999
Chief Laboratory Technician

Education:

University of North Carolina Wilmington
Bachelors, Biology

Skills:

Supply Chain Management, Validation, Quality System, 21 Cfr Part 11, Capa, Change Control, Fda, Gxp, Gmp, Lims, Computer System Validation, Glp, Sop, Biotechnology, V&V, Trackwise, Quality Agreements, 21 Cfr Parts 210 and 211, Biopharmaceuticals, Good Laboratory Practice, Purification, Quality Assurance, Standard Operating Procedure, U.s. Food and Drug Administration, Corrective and Preventive Action

Possible Relatives

Laura A Stamps Laura K Standifer Laura B Stanfield Laura C Joiner Laura C Stanger Laura M Stanton Laura B Staub Laura T Staudt Laura E Steadman Laura J Whitehurst

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