Mohammad Aminul Hoque

Mohammad Aminul Hoque Email and Phone Number

Senior Manager Quality Control @ NIPRO JMI Pharma Ltd.
Dhaka, BD
Mohammad Aminul Hoque's Location
Dhaka, Dhaka, Bangladesh, Bangladesh
About Mohammad Aminul Hoque

• To plan and monitor all the QC & Microbiology activities in respect to implementation of cGMP

Mohammad Aminul Hoque's Current Company Details
NIPRO JMI Pharma Ltd.

Nipro Jmi Pharma Ltd.

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Senior Manager Quality Control
Dhaka, BD
Mohammad Aminul Hoque Work Experience Details
  • Nipro Jmi Pharma Ltd.
    Senior Manager Quality Control
    Nipro Jmi Pharma Ltd.
    Dhaka, Bd
  • Nipro Jmi Pharma Ltd.
    Senior Manager Quality Control
    Nipro Jmi Pharma Ltd. Jan 2023 - Present
    Chauddagram, Cumilla
  • Nipro Jmi Pharma Ltd.
    Quality Control Manager
    Nipro Jmi Pharma Ltd. Mar 2017 - Dec 2022
    Chauddagram, Cumilla
  • Square Pharmaceuticals Limited
    Sr. Executive, Quality Control
    Square Pharmaceuticals Limited Sep 2016 - Feb 2017
    Bangladesh
    ·       Organized sampling of raw materials, bulk products, packaging materials, water sample.·       To organize and supervise analytical activities of water, raw materials, packaging materials and finished products.·       Preparation/review of specification and method for of raw materials, packaging materials and finished products.·       Manage Resources and laboratory inventory control like method, working standard, CRS, column reagents and Instruments·       Preparation of… Show more ·       Organized sampling of raw materials, bulk products, packaging materials, water sample.·       To organize and supervise analytical activities of water, raw materials, packaging materials and finished products.·       Preparation/review of specification and method for of raw materials, packaging materials and finished products.·       Manage Resources and laboratory inventory control like method, working standard, CRS, column reagents and Instruments·       Preparation of Instrument method, sequence and projects·       Solve the analytical problem and troubleshooting of Instrument.·       To Handle Out of Specification Result (OOS), LIR, QIR and Planned Deviation.·       To Organized Analyst Validation·       To review and update SOPs, EOPs & ECPs as per regulatory requirements.·       To ensure IQ, OQ & PQ of new analytical instruments.·       To raise requisition, evaluate quotation & justification of Instruments, consumable items & Lab spare parts.·       To organize disposal of working standard and test samples after analysis.·       To ensure GLP and chemical safety in every steps of laboratory activities.·       To train up newly joined employee (e.g.: Executive, Officer, Analyst, Sampler and Lab Attendant).·       To communicate with relevant section/department (e.g.: QA, Production, R & D, Engg, RA, PPIC, Warehouse, TSD, SCM, etc) for smooth operation Show less
  • Square Pharmaceuticals Limited
    Sr. Executive, Ard ( Analytical Method Development And Validation)
    Square Pharmaceuticals Limited Jan 2013 - Sep 2016
    Bangladesh
    ·       Supervise and provide necessary guidance for Analytical method development for ANDA (USA) filling, different regulatory market (EMCURE, UK, Malaysia, African countries, TGA, WHO etc.)  and local market products (Solid doses, Ophthalmic solutions, Ophthalmic suspension, MDI, Nasal Spray, Tripocal Spray, Insulin)·       Communication and Handling for tool manufacturing products like EMCURE (US market), EMCURE (UK market), Cerovene Projects (US market)·       Review specification… Show more ·       Supervise and provide necessary guidance for Analytical method development for ANDA (USA) filling, different regulatory market (EMCURE, UK, Malaysia, African countries, TGA, WHO etc.)  and local market products (Solid doses, Ophthalmic solutions, Ophthalmic suspension, MDI, Nasal Spray, Tripocal Spray, Insulin)·       Communication and Handling for tool manufacturing products like EMCURE (US market), EMCURE (UK market), Cerovene Projects (US market)·       Review specification and method preparation for the above mentioned doses form.·       Supervised and provide necessary guidance for Pre-validation of new method developments like recovery study, linearity, LOQ/LOD, precision.·       Supervise and review for Analytical method Validation like assay, Impurities, content uniformity, dissolution, residual solvents.·       Analytical method transfers to Quality Control Department through protocol and report with complete package.·       In-Vitro comparative dissolution study to development the bio-equivalence formulation.·       Stability study for formulation development trial products upto process optimization batches.·       Cleaning method development and pre-validation study, like swab recovery, rinse recovery from different surface plate, plastic, metallic equipments, gasket etc.·       Cleaning method validation and transfer to commercial Quality Control Department.·       Cleaning validation protocol and report preparation (Equipments wise) like manufacturing equipment surface area calculation, diagram drawing, MACO calculation.·       Preparation of standard operating procedure (SOP), Equipment Operating Procedure (EOP),·       To establish and implement effective quality management system·       Handling of quality Incident in a team and product complaint.·       Participate in training session and ensure the implementation. Show less
  • Square Pharmaceuticals Limited
    Executive Quality Control
    Square Pharmaceuticals Limited Mar 2008 - Dec 2012
    Bangladesh
    Perform Cleaning Validation activities i.e. LOD/LOQ determination, recovery study, MACO calculation, Determination of product matrix, Determination of Surface area, sampling, analysis etc.·       Method Trial/tuning/optimization for the finished products.·       Comparative Dissolution testing with innovator product for bioequivalence study.·       Conduct Process validation/ development activities i.e. sampling, analysis of bulk/ intermediate/ finished product sample, documentation… Show more   Perform Cleaning Validation activities i.e. LOD/LOQ determination, recovery study, MACO calculation, Determination of product matrix, Determination of Surface area, sampling, analysis etc.·       Method Trial/tuning/optimization for the finished products.·       Comparative Dissolution testing with innovator product for bioequivalence study.·       Conduct Process validation/ development activities i.e. sampling, analysis of bulk/ intermediate/ finished product sample, documentation and reporting·       Stability related all documentation and analysis·       HPLC/GC column management i.e. Maintain, follow-up for the reconciliation/requisition and requirement for the HPLC/GC columns for stability.·       Export related documentation (stability side)·       Handling of ANDA projects i.e.  Sampling, analysis of bulk/ intermediate/finished product sample, Hold-time study sample analysis, Excipients comparability study sample analysis, Bio-equivalence study (in vivo) documentation and reporting. Show less
  • Coats
    Loboratory Shift Officer
    Coats Dec 2007 - Mar 2008
    Bangladesh
    Received requested sample from customer·                        Match the color with different color shed·                        Prepare a recipe for dyeing through different experiment by combination of color.·                        Send to customer for approval of appropriate color matching
  • Shah Cement
    Quality Control Officer
    Shah Cement Sep 2005 - Dec 2007
    Bangladesh
    ·       Perform the Physical and Chemical analysis of all raw materials, in process materials & finish                         materials and keeping their records.·       Test the Quality Parameters in process & finish goods at the certain interval.·       Checking the weighing factor.·       Maintain the measuring instrument properly & ensure the calibration.·       Ensure proper documentation.·       Perform additional assignments & as and when… Show more ·       Perform the Physical and Chemical analysis of all raw materials, in process materials & finish                         materials and keeping their records.·       Test the Quality Parameters in process & finish goods at the certain interval.·       Checking the weighing factor.·       Maintain the measuring instrument properly & ensure the calibration.·       Ensure proper documentation.·       Perform additional assignments & as and when necessary.·       Perform the Physical analysis (Blaine, Residue, Setting Time, Compressive Strength) of finish                             materials and keeping their records.·       Shift reporting and total Quality Control reporting.  Show less

Mohammad Aminul Hoque Education Details

Frequently Asked Questions about Mohammad Aminul Hoque

What company does Mohammad Aminul Hoque work for?

Mohammad Aminul Hoque works for Nipro Jmi Pharma Ltd.

What is Mohammad Aminul Hoque's role at the current company?

Mohammad Aminul Hoque's current role is Senior Manager Quality Control.

What schools did Mohammad Aminul Hoque attend?

Mohammad Aminul Hoque attended Shahjalal University Of Science And Technology.

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