Highlights:Proficient in all analytical QC related works including Method Development, Method Validation, Method Transfer and evaluation and implementation of cGMP along with data integrity in analytical labs. Gained significant regulatory exposure in handing of US-FDA, EU-GMP, MHRA and ASEAN countries regulatory quires. Quick learner, energetic and motivated, aspiring to become a sound and successful professional in the areas of my interest. Leading analytical activities of QC/Analytical for the last couple of years. Conceptually strong with an innovative and analytical approach to the activities with an eye for details.

Skills:QC Analysis

Goal:Aiming to build up a versatile and challenging career in a positive and dynamic environment where the opportunity to utilize knowledge and experience will be available for professional career development. In such a dynamic organization, I would continuously refine my managerial and analytical skills

Manager,QC 04/2016 - current
The ACME Laboratories Ltd., Dhaka, Bangladesh
Industry: Pharmaceuticals
The Acme Laboratories Ltd. (Plant Address: Dhamrai, Dhaka-1350, Bangladesh). Manager-QC (Head of QC), Cephalosporin Unit
1. Lead all the analytical works of routine analytical testing (Tablet, Capsule, Dry syrup & Dry powder for injection, RM & Packaging materials) with proper documentation. 2. Ensure all Method Validation/verification, Analytical activities for Cleaning validation to face Audit like US-FDA, EU or UK-MHRA etc. 3. Lead and oversee all technical/Analytical issues for Market complain, Tech-transfer, Deviation, CAPA from different sources like, CCR, OOS, LIR, Internal & external Audit, QRM & others to make sure they are complete and accurate. 4. Review and update of all QC/Analytical related documents e.g. SOPs, Trend analysis, Analytical Specifications & Methods of Chemical & Microbiological to facilitate the analytical activities smoothly and efficiently. 5. Supervised Method/Analytical Package transfer/ site transfer activities between lab to lab. 7. QC Assessment and implementation for upcoming new projects and supervise requirements identification, give input to purchase the right equipments and Qualification (IQ, OQ, PQ & SOP/ EOP/ ECP etc) activities of the equipments. 8. Monitor that all QC activities accordingly complying the principles of Company Quality policy, regulatory and cGMP requirements to ensure quality in the product effectively. 9. Devise tactical plan can be collaborately carried out by the team to implement improvements to existing test methods/procedures/technique. 10. Ensure training to Analytical & QC personnel in compliance with the GMP/GLP guidelines and practicing it to build a skilled, knowledgeable, efficient and competent team. 11. Ensure analysts training and supervise proper inventory control of Analytical instruments, spare-parts, glass-wares and reagent/chemicals to control stock and availability. 12. Ensure the CAPA implementation against Laboratory incidence, Internal & external Audit.--

Jahangirnagar University 12/2016 - 12/2018
Dhaka, , Barbados
Degree: Master's Degree
Major:Pharmaceutical Analysis
Masters of Philosophy (M.Phil)

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