VAMSI KRISHNA K

Syracuse

Summary

Detail-oriented Quality Associate with experience supporting Quality Assurance (QA) and Environmental Monitoring (EM) activities in a manufacturing environment. Skilled in collecting and analyzing environmental data, performing material inspection and release, and managing controlled documentation for batch records in compliance with cGMP standards. Proven ability to collaborate with production teams, support audits and investigations, and contribute to process improvements while ensuring adherence to quality and regulatory requirements.

Overview

years of professional experience

Work History

Junior Quality Assurance Analyst

A3 Tech Solutions

Denton, TX

01.2025 - 11.2025

Developed and maintained detailed documentation for test plans, cases, and results to support QA processes.
Executed test cases and process checks to support accuracy, reliability, and regulatory compliance.
Maintained detailed records of test results, defects, and deviations to support audits and batch reviews.
Collaborated with cross-functional teams to report issues and assist in resolving non-conformances.
Analyzed data to identify inconsistencies or potential quality risks and provided recommendations to supervisors.
Supported preparation and review of QA/QC documentation, including batch records and reports.
Contributed to process improvement initiatives to enhance compliance and workflow efficiency

Quality Assurance Analyst

Veras Pharmaceuticals Pvt Ltd

Andhra Pradesh, India

01.2021 - 10.2022

Performed inspection and verification of materials and components to ensure compliance with quality and safety standards.
Coordinated Environmental Monitoring (EM) activities, including data collection, analysis, and reporting for controlled production areas.
Reviewed equipment cleaning, area clearance, and production readiness documentation prior to start-up.
Assisted in preparing and reviewing batch records, SOPs, and other controlled documentation for regulatory compliance.
Supported audits, investigations, and risk assessments, providing documentation and follow-up on corrective actions.
Monitored charts, gauges, and process parameters to ensure equipment and processes operated within specification.
Trained production staff on GMP, aseptic techniques, and company quality procedures to ensure compliance.
Participated in process improvement projects to enhance quality, efficiency, and compliance within production workflows.

Education

Master of Science - Bio Medical Health Informatics

SUNY OSWEGO

Syracuse, NY

12-2024

ORAQ Regulatory Affairs Training Program -

Duke University School of Medicine

Bachelor of Science - Pharmacy

Nirmala College of Pharmacy

Vijayawada, India

07-2022

Skills

Quality & Compliance: GMP, GDP, CAPA, Root Cause Analysis, Risk Assessment, Audit Support, Batch Record Review
Environmental Monitoring: Sampling, Data Analysis, EM Reporting
Documentation & Systems: SOP Writing & Review, Document Control, TrackWise, MasterControl, Veeva Vault

Tools: MS Excel, Word, PowerPoint, SAP, Microsoft SharePoint
Soft Skills: Attention to Detail, Communication, Team Collaboration

Timeline