Adithya S Email & Phone Number

North York, Ontario, Canada

• Performing auditing activities on manufacturing and packaging processes for Cosmetic and Over-the-counter products to ensure they meet specific requirements based on SOP, GMP, GDP, FDA and Health Canada regulatory.
• Reviewing and release of batch records and fill sheets to ensure GDP and cGMP.
• Recording Audit results and updating the system on a timely basis.
• Completing line clearance for manufacturing and filling process in compliance with SOP.
• Conducting AQL… Show more Performing auditing activities on manufacturing and packaging processes for Cosmetic and Over-the-counter products to ensure they meet specific requirements based on SOP, GMP, GDP, FDA and.
• Conducting AQL inspection and 100% inspection to ensure the quality and quantity of the finished and pre-finished products.

Edgeware Brampton Canada

• Inspection of Johnson & Johnson client’s products in compliance with SOP, protocol, GMP, GDP and Health Canada regulatory guidelines.
• Performing work order approval and reviewing documents related to shipping, releasing, and receiving based on the SOP and Safety Management plan (ZenQMS).
• Ensuring the quality of products through regular inspections.
• Identifying any deviation during the packaging process and reporting it to supervisors.
• Supporting activities associated with… Show more Inspection of Johnson & Johnson client’s products in compliance with SOP, protocol, GMP, GDP and Health Canada regulatory guidelines.
• Supporting activities associated with precursor products.

Montreal, Quebec, Canada

• Conduct a thorough review and analysis of adverse event reports received from healthcare professionals, patients, and other sources by ensuring regulatory requirement compliance.
• Identifying, analyzing, and interpreting safety data.
• Development and maintenance of standard operating procedures (SOPs) and working instructions toensure compliance with global safety regulations.
• Designing Case Report Form (CRF), Filling up the patient’s history in the CRF, and lab results… Show more
• Designing Case Report Form (CRF), Filling up the patient’s history in the CRF, and lab results dataentry.
• Creating protocol synopsis and analyzing regulatory requirements.

Thiruvananthapuram, Kerala, India

• Worked on project Molecular screening of sweet potato genotype by proteinase inhibitor gene against sweet potato weevil infestation.
• Prepared the protocol and conducted the experiments.
• Prepared and documented daily progress, lab work and risk assessment.
• Assisted and coordinated the material and chemical purchase.
• Monitored project status and ensured the GCP and GMP.
• Performed routine laboratory procedures including Isolation of RNA, quantification of RNA-nano drop,… Show more

Kollam, Kerala, India

• Worked on project Isolation and characterization of phenol degrading bacteria from industrial soil.
• Observed and recorded the experiments at every stage.
• Collection, and management of data.
• Sample collection and media preparation.
• Conducted laboratory procedures including serial dilution, platting, gram staining, microbial characterization, and Biochemical assays (Indole test, Methyl red test, Voges-Proskauer test, Citrate test, Starch.
• Conducted laboratory procedures including serial dilution, platting, gram staining, microbial characterization, and Biochemical assays (Indole test, Methyl red test, Voges-Proskauer test, Citrate test, Starch.

Post Graduate Diploma, Clinical Research

Master'S Degree, Biotechnology

Bachelor'S Degree, Botany And Biotechnology