Highly driven medical science enthusiast with a Doctor of Pharmacy degree from India. Currently pursuing a Masters in Pharmaceutical Regulatory Affairs (NFQ Level 9) in South East Technological University, Ireland. Hands-on experience working in the Quality department for almost one year in a leading pharmaceutical manufacturing company in Kerala, India. Aim at acquiring more knowledge and skills working in the pharmaceutical and medical device industry ensuring the quality and regulatory requirements in manufacturing and development of different drug products and medical devices, thus giving maximum output for the safety of the community and the organization.
• Ensuring all the activities done in the industry complies to the standard operating procedures and good manufacturing practices.
• Determining and performing best methods and quality control tests of the products being manufactured.
• Ensuring the laboratory and industrial facilities meet the government standards for equipment safety and activity logs.
• Inspecting, calibrating and testing the various equipments to ensure the safety and quality before and after using.
• Preparing and archiving the batch manufacturing record and batch packing record of the various products.
• Regulatory roles such as obtaining approval and licensing of new pharmaceutical products.
• Documentation and reviewing of the standard operating protocols and standard testing protocols of all the equipments and raw materials used.
•Assuring and testing the quality of all the pharmaceutical products and the raw materials used according to the regulatory guidelines.