AYUSH KUMAR KAR
Hyderabad,Telangana
Summary
Quality-driven and detail-oriented IPQA Officer with 2 years of experience in pharmaceutical manufacturing. Proficient in GMP, documentation review, and in-process checks. Seeking to contribute expertise in quality assurance and regulatory compliance to ensure consistent product excellence and support continuous improvement within the organization.
Overview
3
3
years of professional experience
Work History
Officer – IPQA
Granules India Limited
Hyderabad, Telangana
01.2023 - Current
- Conduct routine and non-routine in-process quality checks to ensure compliance with cGMP, EU Annex 1, and ICH guidelines.
- Review executed Batch Production Records (BPRs) and associated documents, ensuring timely deposition to DCQA.
- Monitor shop floor activities and perform line clearance during product changeovers.
- Ensure adherence to ALCOA+ principles in documentation and process verification.
- Monitor environmental conditions and alarm systems.
- Support internal and external audits by maintaining readiness and document control.
Education
M.Pharm - undefined
OUHS
B.Pharm - undefined
Roland College of Pharmaceutical Sciences
01.2023
Skills
- Good Manufacturing Practices (GMP)
- Good Documentation Practices (GDP)
- IPQA Checks
- Deviation Handling
- Documentation Review
- BPR Verification
- Line Clearance
- In-Process Monitoring
- Sampling of Finished Products
- Compliance with GMP
- EU Annex 1
- ICH Guidelines
- Environmental Monitoring
- Alarm Systems
- Audit Support
- Regulatory Readiness
- Knowledge of ALCOA Documentation Principles
Websites
Projects Training
Completed industrial training in the IPQA Department, gaining hands-on exposure to in-process checks, line clearance, and GMP documentation practices.
Timeline
Officer – IPQA
Granules India Limited
01.2023 - Current
M.Pharm - undefined
OUHS
B.Pharm - undefined
Roland College of Pharmaceutical Sciences