For over 22 years Robert Wissert worked in different jobs. Recently, the professional worked as a Consultant in Valsource, Llc developing required skills. Robert graduated from Temple University in 2020 where the professional got all the required skills. This expert has all necessary skills for his job, that's proven by these certifications in Six Sigma Green Belt, Six Sigma Lean Manufacturing, and Six Sigma Black Belt. You can find Robert in Collegeville, Pennsylvania, where he lives nowadays. SoftwareOfficial has all the data you need to be in touch with Robert Wissert, such as Robert Wissert's phone number or e-mail. Send the request to get additional data.
Name variants:
Bob Wissert,
Bobbie Wissert,
Bobby Wissert,
Dob Wissert,
Rob Wissert,
Robbie Wissert,
Robby Wissert,
Robin Wissert,
Bert Wissert,
Bertie Wissert
Last updated Jun 14, 2024
Contact Information
Last Update
Jul 11, 2022
Email
ro**@yoh.com, rw**@valsource.com, ro**@gmail.com
Location
Collegeville, PA
Company
Workplace
Consultant
Downingtown, PA
Industry
Pharmaceuticals, Pharmaceutical Consulting, Nonclassifiable Establishments
Colleagues
Work History
Consultant
918 Horseshoe Pike, Downingtown, PA 19335
Supported projects utilizing the lifecycle validation approach described in FDA’s January 2011 PV Guidance for industry. Knowledgeable in ICH Guidelines and aspects of PDA Technical Report 5...
Jan 1, 2013 — Nov 2015
Manager of Business Development
1500 Spring Garden St, Philadelphia, PA 19130
Manager of Business Development at Yoh, A Day & Zimmermann Company
from Nov 2015
Validation Specialist
600 Montgomery St, San Francisco, CA 94129
Jul 2000 — Jun 2003
Education
2015 — 2020
2015 — 2016
2010 — 2011
2002 — 2002
Occupations
Executive
Manager
Counselor
Operations Manager
Advisor
Skills
Validation
Fda
Gmp
Change Control
V&V
21 Cfr Part 11
Pharmaceutical Industry
Sop
Biotechnology
Capa
Gxp
Cleaning Validation
Cross Functional Team Leadership
Quality Assurance
Manufacturing
Biopharmaceuticals
Quality System
Aseptic Processing
Regulatory Affairs
Medical Devices
Regulatory Requirements
Computer System Validation
Technology Transfer
Glp
Iso 13485
Pharmaceutics
Quality Auditing
Quality Control
Vaccines
Protocol
Lifesciences
Regulatory Submissions
Process Simulation
Trackwise
Root Cause Analysis
Calibration
Gamp
Lims
Sterilization
Minitab
Hplc
Clinical Development
Document Management
R&D
Gcp
Chromatography
Clinical Trials
Cro
Analytical Chemistry