Haridha Kesavan
Compounding Technician, Packing @Baxter International Inc.
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WORK HISTORY
Compounding Technician, Packing @Baxter International Inc.
Oxford, GB
Perform quality checks and package pharmaceutical products accurately and efficiently. Prepare and compound products while ensuring compliance with GMP and internal SOPs. Operate and maintain packing equipment and machinery efficiently. Document production activities and batch records accurately for regulatory compliance. Utilize Merlin software for tracking, batch processing, and reporting. Completed SOJT (Structured On-the-Job Training) for cleanroom operations, gaining hands-on experience in a controlled, sterile environment. Collaborate with team members to optimize workflow and support continuous improvement initiatives. Maintain a clean, safe, and controlled working environment, adhering to all health, safety, and environmental protocols.
EDUCATION
Harvey Biomedical
Advanced training in Biomedical Applications , Medical devices
Dhanalakshmi Srinivasan Engineering College
Bachelor of Engineering - BE, Biomedical/Medical Engineering
De Montfort University
Master of Science - MSc, Pharmaceutical Sciences
ABOUT HARIDHA KESAVAN
Regulatory Affairs professional with 2+ years’ experience in medical devices and IVDR compliance, now pursuing an MSc in Pharmaceutical Quality by Design at De Montfort University, UK. Skilled in global submissions (MDR, FDA, ISO), QMS, CAPA, risk analysis, and vigilance reporting, with hands-on training in HPLC, FTIR, UV-Vis, and tablet compression.Previously at HCL Technologies, I managed 50+ submissions monthly, streamlined workflows to boost efficiency by 25%, and strengthened compliance processes. Passionate about applying QbD principles and regulatory expertise to ensure safe, compliant, and innovative healthcare solutions.
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