Say no to manually filling long application forms
Visit any careers page and a lightning button will pop up on any compatible page with a form
Use ChatGPT to auto-fill job forms
Ask for Referral for any job post
Anshuman Dey
Deputy Manager-Clinical Trial Quality Assurance team, Biocon Biologics
Education Overview
Companies Overview
• biocon biologics
• biocon
• iqvia
• clinogenta unit of gvkbiosciences private limited
• embrace innovations
• cadila pharmaceuticals
• cadila pharmaceuticals ltd
Experience Overview
16.1 Years
Find anyone’s contact
Experience
Deputy Manager-Clinical Trial Quality Assurance team, Biocon Biologics
biocon biologics | Bengaluru, Karnataka, India
2021 - Present
Quality Assurance Auditor-Global Clinical Trial QA team,Quality Assurance Department
iqvia | Bengaluru Area, India
2015 - 2017
Clinical Trial Quality Assurance Auditor-Quality Assurance Department
clinogenta unit of gvkbiosciences private limited | Gurgaon,Delhi NCR, India
2013 - 2015
Team Leader-Clinical Operations,Clinical Affairs Department
embrace innovations | Bangalore,Karnataka,India
2012 - 2013
Assistant Manager-Research Quality Assurance Department-CRO,
cadila pharmaceuticals | Dholka,Ahmedabad,Gujarat,India
2011 - 2012
Research Associate-Research Quality Assurance Department-CRO
cadila pharmaceuticals ltd | Dholka,Ahmedabad,Gujarat,India
2008 - 2010
Skills
Boost your visibility and stand out to employers with referrals from your LinkedIn connections.
21 CFR Part 11
analytics
ANDA
Application Monitoring
Application Programming Interfaces (API)
Artificial Intelligence (AI)
Auditing
auditing
Automation
AWS Lambda
BA/BE study
Bioanalysis
CAPA
Clinical Data Management
Clinical Development
Clinical Monitoring
Clinical Research
Clinical Trials
ClinOne Software application
Consultancy audits
CRF design
CRM
CRO
CTMS
Customer Relationship Management (CRM)
Data Management
Design
Drug Safety
EDC
FDA
GCP
GLP
GMP
Good Clinical Practice (GCP)
Google Cloud Platform (GCP)
HPLC
ICH-E3
ICH-E6
ICH-GCP
IND
ISO 14155
marketing
Medical Devices
Medical Writing
Payments
Pharmaceutical Industry
Pharmaceutics
Pharmacovigilance
quality assurance (QA)
Quality System
Qualty Assurance
Regulatory Affairs
Regulatory Audits
Regulatory Requirements
Research
Research Scientist
Schedule Y
Site Audit
Site Monitoring
SOP
Sponsor audits
Standard Operating Procedure (SOP)
Vaccines
Validation
Contact Details
Email (Verified)
ansXXXXXXXXXXXXXXXXXXXXinMobile Number
+91XXXXXXXX34Education
No data found
Frequently asked questions
Find anyone’s contact and let Weekday reach out to them on your behalf
Start hiring nowStop manually filling job applications. Use AI to auto-apply to jobs
Look for jobs now