Faiyaz Uddin Email & Phone Number

A result oriented & competent professional with an experience of over 23 years in Quality Control and Quality assurance. Proficient in the areas of QA & QC, Regulatory Affairs , Validation , Internal / Vendors / Regulatory Audits and Trainings.An excellent planner and organizer with the ability to manage a staff to reach goals while strictly adhering to budgets and, cGMP, GLP, and ICH and regulatory audits.Well diverse with 21CFR, PIC/S, ICH, WHO GMP, ISO, GLP, Drug and Cosmetic Act Guidelines, Stability studies, Data integrity, SOPs improvements , Quality risk assessment. Expertise in implementation of Good Laboratory Practices & Compliance with Regulations. Performing GAP analysis and Audit report and compliance with CAPA to get Quality unit ready for any regulatory inspections.As a head, leading Technical and Administrative Functions of QA & QC department, Proficient in reviewing Quality Documents and Quality Investigation reports. Business development and support to export and technical support to Customer / Contract manufacturing. Strategic Planning of Sampling, Analysis, Review and Release, QMS Handling, Equipment and Instrument Qualification, analytical method development and analytical Validation of Laboratory and Plant Process, Training and People Development, Dossier Documentation and Audit &Compliance etc. Handling OOS/OOT, incidences, Deviation and change control, CAPA. Cost reduction and safety compliance of the personnel’s.Previously worked with big Pharma Giant companies like Cipla Ltd, Ranbaxy Laboratory Ltd & Mylan Pharma Inc & well aware to handle all regulatory audits i.e WHO,USFDA, TGA, MHRA & MCC.Leading several Country / Clients Audits – YEMEN, ALGERIA , NEPAL , UGANDA , TANZANIA, MERCK,JB CHEMICALS, MSN, SAVA, SHALINA ,TORRENT, GLENMARK.

Listed skills include Validation, Hplc, Gmp, Pharmaceutical Industry, and 30 others.