8.7 years of experience in IT as a CSV Consultant with core competencies in Quality Module applications for pharmaceutical industry.
Specialties
鈥� Validation and Verification of Pharma Processes and applications.
鈥� GAMP 5.0, 21CFR Part 11, GxP, ITIL V3
鈥� Process implementation, Process Consulting.
鈥� Quality/Regulatory Auditing, Application Development & Support.
We鈥檝e updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data.
You can read the details below. By accepting, you agree to the updated privacy policy.
