SIMI THAYYIL ANIL

Pharmaceutical and Clinical Professional with a Doctor of Pharmacy (PharmD) and an MSc in Pharmaceutical Science (UK), with specialisation in Health and Disease of Physiological System. Experienced across quality assurance, quality control, regulatory affairs, research, and pharmacy operations within both industry and healthcare settings. Hands-on experience with GMP, GLP, GCP, SOP compliance, regulatory documentation (CTD/eCTD), and analytical techniques including HPLC, UPLC, GC-MS, UV-Vis, TLC, and Karl Fischer titration. Proven ability to support sample testing, analytical data interpretation, scientific reporting, batch documentation, audits, inspections, and patient-safe dispensing, while maintaining high standards of accuracy, data integrity, and compliance. Adaptable professional with strong analytical, documentation, research, and communication skills, seeking roles within the UK pharmaceutical, quality, laboratory, or pharmacy sectors.

• GMP, GLP, GCP compliance
• SOP development and adherence
• Regulatory submissions (CTD/eCTD)
• Batch documentation and CoA review
• Quality assurance and quality control
• Pharmacovigilance fundamentals
• Stability studies & data review

• HPLC, UPLC, GC-MS, UV-Vis
• Karl Fischer titration
• Sample preparation and analysis
• Method development and validation (supporting level)
• Analytical data interpretation and reporting

Clinical Pharmacist Intern

Tiruppur Government Hospital (Medical College), India 

(One-year clinical internship)

• Completed a one-year clinical pharmacy internship in a tertiary care government hospital setting.
• Participated in clinical rounds, prescription review, and medication therapy management under supervision.
• Provided patient counselling and supported safe medication dispensing in accordance with hospital protocols.
• Assisted in drug utilisation reviews, documentation, and maintenance of accurate pharmacy records.

NVQ Level 2 in Pharmacy Services (UK)