Khairul Alam

Deputy Manager,Validation at Beacon Pharmaceuticals Limited
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Contact Information
us****@****om
(386) 825-5501
Location
Dhaka, Bangladesh, BD

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5.0

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/ Based on 2 ratings
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Md. Rakibul Islam

Mr. Alam is a natural leader. If you want to be motivated, you might want to talk to Mr. Alam. He will not tell you some buzz words and send you on your way, no, he will ask you questions, learn about the situation you are in and then he will tell you what you should do to improve your situation and he will also tell you about the other side. This educated situation analyzing ability has given Mr. Alam a subliminal power to manage his subordinates and solve complex inter and intra-departmental problems. Beside being a leader, he also has expertise in managing Quality Risks, performing Validation and Qualification processes, acting as a GMP Inspector and also in other aspects of quality assurance.

Masud Perves

Mr. Khairul Alam and I both working at Renata Limited. I found Mr. Khairul a self starter, habituated to work independently as well as in team and lastly very respectful to his duties and responsibilities. He is skilled on Pharmaceutical Quality Compliance, QMS (Quality Management System) and documentation. He also worked for Qualification, Process validation and cleaning validation. He has received a number of training both on QMS and Validation. I highly recommend Mr. Khairul to work in industry both in validation and Quality Assurance areas.

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Experience

    • Bangladesh
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Deputy Manager,Validation
      • Oct 2019 - Present

    • Bangladesh
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Deputy Manager
      • Mar 2019 - Sep 2019

    • Bangladesh
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Additional Manager,Quality Assurance Department
      • Sep 2008 - Jan 2019

      Major Responsibilities: Regular inspection of the plant to ensure that good house-keeping and approved procedure are being practiced to ensure that at all times it meets the standards of cGMP.Design, develop, implement, monitor and control overall documentation system and as per the GMP requirements.Documenting and giving technical support (Where needed) to all the validation activities including process validation, cleaning validation and the qualification (i. e. IQ, OQ, and PQ protocol and report) of all process equipment. Generating all the required documents for production i. e. Formulation Order (FO), Fill Label Pack (FLP), Batch Manufacturing Record (BMR), Batch Packaging records (BPR). Generating and implementing all GMP related SOPs.Controlling and distribution the SOPs of all departments.Evaluate the Batch Production Records and Quality Control Record and preserve them along with the control samples at specified period and ensuring the tractability of manufactured products. Ensuring that the manufactured products are inspected and all stages as per norms.Compilation and controlling the deviation and change control reports.Organizing and performing self-inspection and also to submit report on findings to respective authority and to take part in the follow up action.Ensuring required initial and continuous training of production/plant personnel is carried out according to the need.Generating annual product review report.Identifying the requirement of any significant change required in relevant department about it.Handling product complaints.Responsible for all Audits activities for the plant.Enhance existing quality systemsMotivate subordinates.Any other relevant duties assigned by the Q. A. Manager.Also have the experience to work in Quality Control Laboratory and preparing dossier in ACTD & CTD format.

Education

  • Jahangirnagar University
    M.S., Biochemistry & Molecular Biology
    2005 - 2006
  • Jahangirnagar University
    Bachelor's degree, Biochemistry and Molecular Biology
    2000 - 2004

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