Ritwik Majumdar
Associate Ii @Alcon
Signup · Get unlimited contacts
WORK HISTORY
Associate Ii @Alcon
Bengaluru, IN
1.Responsible for on time submission of Medical Device regulatory reports to different Health Authorities.2.Complaint Handling and event coding.4.Writing medically cohesive clinical narratives.5.Gather information required for review and reportability of complaints according to SOPs.6.Complete all needed records within the timeframe.7.Assess if the risk assessment is covering the hazard in the complaint.8.Communicate with customers, call center reps and field engineers to gather more data on complaints.9.Closing the complaints with accuracy by following SOPs.10.Complete daily and weekly objectives consistently month on month.11.Reconciling reports to achieve perfection in daily activities.12.Performing investigation activities for medical devices in accordance to 21 CFR.
EDUCATION
West Bengal University of Technology, Kolkata
Bachelor of Pharmacy - BPharm
ABOUT RITWIK MAJUMDAR
B.Pharma graduate, working as a Medical Device Safety & Vigilance Associate.PROFESSIONAL STRENGTHS INCLUDE. ISO 13•••21CFR 820. 21 CFR 803. Regulatory Authorities Report Submissions. Product reliability and Customer Complaints. Quality Management
This profile is compiled from publicly available professional sources. Unifers is not affiliated with or endorsed by LinkedIn. Request removal of this profile.