Rama Tyagi
Vice President, Quality and Regulatory Affairs and Acting Chief Operations Officer
Rama Tyagi is a eficient professional, who works in Liquid Genomics on the position of Vice President, Quality and Regulatory Affairs and Acting Chief Operations Officer since 2015. Rama Tyagi gained professional experience in more than eight positions at various companies. Rama Tyagi went to the California State University - Dominguez Hills and received education from 2002 to 2006. Rama has such professional qualifications as State of California and Clinical Laboratory Scientist. Los Angeles, California is the city, where this expert was lastly known to be located. This expert's email address and phone can be easily accessed through this website on demand.
Name variants:
Rama Tyagi
Contact Information
Last Update
Jul 9, 2022
Email
sp**@ca.rr.com, rt**@neurosystec.com
Location
Los Angeles, CA
Company
Liquid Genomics
Workplace
Vice President, Quality and Regulatory Affairs and Acting Chief Operations Officer
Work History
Vice President, Quality and Regulatory Affairs and Acting Chief Operations Officer
Provide leadership to develop and maintain a Quality system (QMS), compliant to International, FDA, CLIA, State and local regulatory bodies and implement Billing processes and policies accor...
May 2015 — Jan 2018
Director, Quality and Regulatory Affairs
Los Angeles, CA
Provide Regulatory support to validate assays, compliant to New York Standards and submit those to NYS DOH for approval.
Prepare sponsored studies data for FDA submission and inspection.
...
Jan 2013 — Apr 2015
Director, Quality and Regulatory Affairs
11915 La Grange Ave, Los Angeles, CA 90025
Creation of a quality and regulatory department to integrate into the corporate culture of the firm, no previous department of this type previously existed. A thorough and complete knowledge...
Jan 2010 — Nov 2012
Director, Quality and Regulatory Affairs
Leading systems (including quality control activities, design control, vendor qualification, document control, auditing and monitoring, risk-benefit analysis, NCR & CAPAs) and regulatory sub...
Dec 2006 — Dec 2009
Quality and Regulatory Manager
Responsible for managing the regulatory/quality system activities for both analytical (clinical trial) and diagnostic divisions.
Ensured quality systems supported both federal and local qu...
Oct 2002 — Oct 2006
Quality and Regulatory Affairs Manager
NeuroSystec develops fully implanted drug delivery devices for delivering drugs to the ear to treat tinnitus.
Education
Occupations
Executive
Director
Scientist
Biotechnology Professional
Leader
IT Professional
Software Tester
Operations Manager
Biologist
Biological Scientist
Managers
Computer Specialist
Skills
Fda
Biotechnology
Medical Devices
Microbiology
Clinical Research
Quality System
Lifesciences
Quality Management
Validation
Process Improvement
V&V
Gmp
Quality Assurance
Clinical Trials
Regulatory Affairs
Pharmaceutical Industry
Regulatory Submissions
Glp
Sop
Immunology
Ctms
Technology Transfer
Pharmaceutics
Gcp
Quality Control
Gxp
Iso
21 Cfr Part 11
Drug Development
Molecular Biology
Capa
21 Cfr
Healthcare
Clinical Development
Change Control
Biopharmaceuticals
R&D
Design Control
Oncology
Quality Auditing
Aseptic Processing
Cross Functional Team Leadership
Cro
Laboratory
Regulatory Requirements
Iso 13485
Pma
Ind
Cmc Regulatory Affairs
Computer System Validation
Life Sciences
U.s. Food and Drug Administration
Standard Operating Procedure