Devansh Kansara Email & Phone Number

Toronto, On, Ca

Mississauga, Ontario, Canada

• Medication Dispensing: Within the guidance of a professional pharmacist, precisely prepare and dispense prescription drugs while adhering to all safety and legal requirements.• Interaction with Patients: Deliver outstanding customer service by helping patients with prescription queries, prescription guidelines and suggestions for over-the-counter goods.• Inventory management: Keep track of expiration dates, maintain and monitor pharmacy inventory levels, and make sure prescriptions are stocked and arranged correctly.• Prescription Processing: Carefully review and process prescription orders, confirm patient details, and enter data into the pharmacy's computer system.• Labeling and Packaging: Comply with safety and regulatory regulations while labeling and packaging prescription vials, bottles, and blister packs.• Insurance Claims: Help patients submit prior authorizations and insurance claims while making sure that all billing and documentation are done correctly.

Greater Toronto Area, Canada

Gandhidham, Gujarat, India

• Have successfully faced USFDA inspection with zero deficiency from analytical laboratory. • Basic knowledge and experience of HPLC, LC-MS.• Have experience in preparing reports and protocols.• Familiar with ALCOA, ICH and USFDA guidelines.• Knowledge in cGMP and cGLP compliance.• Proficient in troubleshooting and operating HPLC, TLC, KF-Titration and PH meter. • Safe disposal of waste solvent as per the SOP and cGMP requirements.• Having sound theoretical knowledge and understanding of FT-IR and Chromatography. • Stability study and force degradation study for assay for assay and related substance method development.• Investigation study with Out of Specification, CAPA documentation and Trend Analysis.• Highly dedicated towards maintaining high quality standards in documentation. • Arranging reference standard database with Certificate of Analysis.• Familiar with the concept of GC-MS, LC-Ms

Gandhidham, Gujarat, India

schedules.• Created and updated Standard Operating Procedures (SOPs) to align with production process requirements and quality control standards.• Approval and reviewed the BMR (Batch Manufacturing Record), ensuing accuracy and compliance with the cGMP regulations and SOP’s. Conducting quality inspection and release of raw material and finished products, maintaining high standards of quality.• Established and maintained positive working relationships with internal and external stakeholders to facilitate efficient workflow.• Prepared various quality documents, including specifications and Certificates of Analysis (CoA) for finished products.• Reviewed product labels during design, printing, and receipt stages to ensure compliance with regulatory standards.• Maintained various QA documents and records, ensuring completeness and accuracy.

Master'S Degree, Regulatory Affairs

Masters, Pharmaceutical Sciences, 8.3 Cgpa

Gold medalist in Pharmaceutical Analysis, Analytical method Validation for separation of novel triple combination of Amlodipine Besylate.

Mpharm, Pharmaceutical Analysis, 8.87 Spi

Activities and Societies: Two Research articles published: 1. In Springer Journal 2. Journal of Chemical Metrodology

Bachelor Of Pharmacy, Pharmacy, 7.77

Activities and Societies: Pharmavision- Marketing competition winner, badminton