Thomas P Lenzi, Age 597 Wardell Rd, Livingston, NJ 07039

Thomas Lenzi Phones & Addresses

7 Wardell Rd, Livingston, NJ 07039 (973) 992-4609 (973) 992-6609

10 6Th Ave, Seaside Heights, NJ 08751 (732) 793-1397 (732) 854-1661 (732) 854-8779

3404 Jefferson Ave, Toms River, NJ 08753 (732) 573-9724 (973) 992-4609

10 6Th Ave, Dover Township, NJ 08753 (732) 854-1661 (732) 793-1397 (732) 854-8779

Ocean, NJ

7 Wardell Rd, Livingston, NJ 07039 (201) 314-2456

Social networks

Thomas P Lenzi

Linkedin

Work

Company: Novartis Sep 2001 to Dec 11, 2016 Position: Associate director - clinical quality assurance

Education

School / High School: Seton Hall University School of Law 2009 to 2011 Specialities: Law

Skills

21 Cfr Part 11 • Gxp • Computer System Validation • Pharmaceutical Industry • Quality Assurance • Clinical Trials • Fda • Validation • Clinical Development • Gcp • Sop • Regulatory Submissions • Capa • Regulatory Affairs • Drug Development • Cro • Pharmacovigilance • Gmp • Biopharmaceuticals • Regulatory Requirements • Quality System • Glp • Technology Transfer • V&V • Lims • Risk Assessment • Gamp • Quality Auditing • Corrective and Preventive Action • Verification and Validation • Good Clinical Practice

Languages

English

Emails

Industries

Pharmaceuticals

Mentions for Thomas P Lenzi

Thomas Lenzi resumes & CV records

Resumes

Thomas Lenzi Photo 14

Associate Director, Clinical Quality Assurance

Location:
7 Wardell Rd, Livingston, NJ 07039
Industry:
Pharmaceuticals
Work:
Novartis Sep 2001 - Dec 11, 2016
Associate Director - Clinical Quality Assurance
Creon Software Aug 1998 - Sep 2001
Project Manager
Ciba-Geigy May 1987 - Jul 1998
Quality Assurance
May 1987 - Jul 1998
Associate Director, Clinical Quality Assurance
Education:
Seton Hall University School of Law 2009 - 2011
Seton Hall University 2000 - 2005
Master of Business Administration, Masters, Finance
Muhlenberg College 1982 - 1986
Bachelors, Bachelor of Science, Chemistry
Skills:
21 Cfr Part 11, Gxp, Computer System Validation, Pharmaceutical Industry, Quality Assurance, Clinical Trials, Fda, Validation, Clinical Development, Gcp, Sop, Regulatory Submissions, Capa, Regulatory Affairs, Drug Development, Cro, Pharmacovigilance, Gmp, Biopharmaceuticals, Regulatory Requirements, Quality System, Glp, Technology Transfer, V&V, Lims, Risk Assessment, Gamp, Quality Auditing, Corrective and Preventive Action, Verification and Validation, Good Clinical Practice
Languages:
English

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