We found the following information about Leta Sledge at Delta Project Management, where the professional has worked as a Regional Validation Manager since 2020. Leta's total work experience is over 12 years, during which time this person had at least ten jobs at different companies to develop professional skills. Leta studied at the Drexel University from 2000 to 2003. Leta Sledge currently lives in Philadelphia, Pennsylvania. You can contact with Leta by searching for phone number or email or get additional information by requesting access to Leta Sledge's additional details from SoftwareOfficial.
Name variants:
Leta Sledge
Last updated Jun 03, 2024
Contact Information
Last Update
Jul 5, 2022
Email
le**@hotmail.com, le**@ptd.net, le**@yahoo.com
Location
Philadelphia, PA
Company
Workplace
Regional Validation Manager
San Francisco, CA
Industry
Biotechnology, Engineering Consulting Services, Management Services
Colleagues
Work History
Regional Validation Manager
400 Concar Dr, San Mateo, CA 94402
from Jan 2020
Validation Project Manager
6260 Lookout Rd SUITE 120, Boulder, CO 80301
from Feb 2016
Senior Validation Consultant - Consent Decree
8334 Veterans Hwy, Millersville, MD 21108
Jan 2013 — Jan 2016
Senior Cleaning and Sterilization Validation Consultant
1500 Spring Garden St, Philadelphia, PA 19130
May 2012 — Jan 2013
Validation and Quality Systems Consultant
8235 Forsyth Blvd Suite 900 St, Louis, MO
Validation and Quality Systems Consultanting
Oct 2010 — Feb 2011
Validation Engineer
7451 Keebler Way, Allentown, PA 18106
Nov 2006 — Feb 2009
Validation Coordinator
14 Schoolhouse Rd, Somerset, NJ 08873
Sep 2004 — Nov 2006
Biomedical Equipment Technician
3400 Spruce St, Philadelphia, PA 19104
Jun 1998 — Sep 1998
Education
2000 — 2003
1998 — 1999
Occupations
Executive
Manager
Project Manager
Operations Manager
Project Managers
Skills
Validation
Quality System
Cleaning Validation
Fda
Capa
Gmp
Change Control
Computer System Validation
Pharmaceutical Industry
V&V
Quality Assurance
21 Cfr Part 11
Iso 13485
Aseptic Processing
Gxp
Biopharmaceuticals
Sop
Technology Transfer
Gamp
Lean Manufacturing
Quality Control
Manufacturing
Quality Auditing
Regulatory Affairs
Trackwise
Technical Writing
Continuous Improvement
Biotechnology
Medical Devices
Glp
Lims
Change Management
Pharmaceutics
Verification and Validation
Remediation
Process Simulation
Root Cause Analysis
Corrective and Preventive Action
R&D
Design Control
Calibration
Iso
Design of Experiments
Laboratory
Quality Management
Gap Analysis
Process Validation
Lean Six Sigma
Quality Systems
Cgmp
Six Sigma