Md. Ariful Alam Nishan

Experience

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  E-TEC Ltd

  Jan 2011 - Jan 2012

  Marketing executive sales and services

  As an Executive Sales and Service at E-Tec Ltd, I managed client relationships and facilitated the distribution of BASF chemical products. My responsibilities included ensuring client satisfaction, providing technical support, and optimizing sales strategies to meet business objectives. Through effective communication and problem-solving skills, I contributed to the success of product sales and customer retention initiatives.

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  KNIT CONCERN LTD

  Apr 2012 - Sept 2015

  Chemist and ECR [environmental chemical responsible]

  Chemical Safety & Compliance: Ensure adherence to safety standards and proper handling, storage, and disposal of chemicals.Environmental Impact Monitoring: Monitor and reduce the environmental footprint by complying with regulations on waste and emissions.Quality Control & Product Safety: Oversee chemical testing and application, ensuring product safety and quality standards are met.R&D for Sustainable Solutions: Research and develop eco-friendly chemical alternatives, optimizing processes for better performance and reduced impact. Show less

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  TECHNO DRUGS LTD

  Sept 2015 - Mar 2016

  Quality Control Officer(Microbiology)

  Responsibilities:1. To perform Environmental monitoring of clean rooms (under USP specifications)2. To perform various microbiological testing procedures such as media qualifications, sterilizations, growth promotion tests, validations, identification tests and bioassay. 3. To perform bioburden test, microbial limit test, sterility and endotoxin testing of raw materials, in-process samples, bulk and finished products and stability samples.

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  Eskayef Pharmaceuticals Ltd.

  Apr 2016 - now

  Dedicated Pharmaceutical Analytical Laboratory Procurement SpecialistAccomplished professional with expertise in sourcing, negotiating, and procuring laboratory items, including reagents, instruments, and consumables, for pharmaceutical analytical laboratories. Demonstrated success in ensuring timely deliveries, optimizing inventory management, and maintaining strict compliance with regulatory standards. Certified GMP auditor with SKF, bringing in-depth knowledge of Good Manufacturing Practices to ensure quality and adherence across procurement processes. Experienced in leveraging SAP for efficient procurement and inventory management, streamlining operations, and driving cost-effective solutions. Known for strong communication and negotiation skills, with a passion for advancing the success of analytical laboratories through strategic and efficient procurement practices. Show less Dedicated professional specializing in pharmaceutical analytical laboratory procurement. Expert in sourcing, negotiating, and purchasing laboratory items. Proven track record in ensuring timely deliveries, managing inventory, and maintaining compliance with regulatory standards. Strong communication and negotiation skills, coupled with a deep understanding of pharmaceutical analytical items [reagents, instruments and consumables]. Passionate about contributing to the success of analytical laboratories through effective procurement strategies. Show less Key responsibilities:1. To implement all relevant procedures described in the Quality Management System (QMS).2. To review and approve analysis of Finished Product, pellets, packing material, intermediate, IPQC sample, Stability sample & Raw Material.3. To represent Quality control Department to all external audits from Customers & regulatory authorities. To conduct GMP Audits as per yearly schedules. Other duties & responsibilities1. To report quality system performance metrics including trends, that help decision-making and taking proactive targeted actions.2. To review any document as per instruction of Quality Control Manager, that gives work instructions and set requirements such as procedures, protocols, test methods, and specifications—including changes to these documents. 3. To review and ensure that, laboratory testing of components, containers, in-process materials, packaging materials and drug product are performing by using validated methods against scientifically-derived, fit-for-purpose specifications. 4. To review and ensure the integrity of quality control laboratory data through LIMS. Executing computer system validation documentation (Validation Plan, URS, FRS, IQ, OQ, PQ, RTM, summary report).5. To perform review and approve/reject production batch records and making the final decision to release a product lot into commerce.6. To perform investigation of nonconformance and to confirm root cause is eliminated for failure to meet specification including quality attributes.7. To perform retests or re-examine approved components, drug product after long storage or exposure to adverse conditions.8. To follow the cleaning, safety/ health and security regulations & to perform duties as per current GLP/GDP/cGMP.9. As an independent reviewer, to ensure there is no conflict of interest between regulatory responsibilities and actual daily activities through keeping management informed on product, process and system risks. Show less Performing sampling, analysis, Testing, release, related documentation and other related Quality control functions in respect of Raw material, Packaging materials, Finished goods, in process, Validation and stability samples.Job Responsibilities1. To sample the Incoming RM/Packaging material.2. To conduct analysis and testing of RM/PM/FG/actives and intermediates with the help of analytical instruments and techniques.3. To calibrates/verifies analytical instruments/balances4. To Trouble shots analytical instruments5. To coordinates and follows up with engineering dept for timely availability of their services to attend breakdowns. Interruptions and scheduling of maintenance.6. To review and update raw material and packaging material specifications7. To prepare testing specifications.8. To prepare, review and update working standards.9. To maintain calibration records of instruments.10. To prepare trend analysis of finished products.11. To perform Chemical assays and standardizations of reagents.12. To prepare SOPs, reviews for biannual review. Prepare Training outlines.13. To maintain and control inventory of Reagents. Chemicals/glass wares.14. To conduct stability studies of reagents.15. Prepares analytical reports and certificates of analysis.16. To validate instruments, equipment’s, processes, analytical methods.17. To prepare and evaluate stability data18. To prepare stability protocols Show less

  • Deputy Manager Quality Control [Procurement]

    Jan 2025 - now

  • Senior Assistant Manager Quality Control [Procurement]

    Jan 2024 - now

  • Senior Assistant Manager

    Jan 2022 - Jan 2024

  • Assistant Manager Quality Control

    Jan 2020 - Dec 2021

  • Senior Quality Control Executive

    Jan 2018 - Dec 2019

  • Quality Control Executive

    Apr 2016 - Dec 2017