SƠ YẾU LÝ LỊCHThông tin liên hệ:Tên đầy đủ: SAMAL MUSA (cách MINH SANG)Địa chỉ-1: 157A1/40 Dương Ba Trac Street, Phường 1, Quận 8, TP. Hồ Chí Minh – Việt NamĐịa chỉ-2: 157/22/11/36 Dương Ba Trac, Phường 1, Quận 8, TP. Hồ Chí Minh – Việt Nam Di động: (+ 84) - 0934830092 Viber: (+ 84) - 01224924004Thư điện tử: samalmusa@yahoo.comThông tin cá nhân: Ngày sinh: 20 tháng mười một 1985 Giới tính: Nam Tình trạng hôn nhân: lập gia đìnhBằng cấp: Quản lý/chuyên nghiệp dược và khoa học.Kinh nghiệm làm việc:2013-2014: R & D chuyên gia tại BECAMEX dược phẩm.2010-2013:Sản xuất quản lý tại Savipharm J.S.C– tân thuậnKhu công nghiệp, Quận 7, TP. Hồ Chí Minh, Việt Nam.-Quản lý sản xuất.-Lập kế hoạch sản xuất.-Đảm bảo chất lượng sản phẩm.-Đảm bảo mục tiêu sản xuất.-Phối hợp với kế hoạch, nhà kho, QA, QC, RD, kỹ thuậtBộ phận để đảm bảo các mục tiêu về thời gian.-Dịch các tài liệu, chuẩn bị, xem xét, Cập Nhật Sop, Nhật ký hàng hải-Quen thuộc với GMP-WHO, GMP-Nhật bản, PIC/S, EHS, NẠC,5, KPI, 6 Sigma, rủi ro / quản lý thay đổi... vv...-Sản xuất quản lý bởi hệ thống SCADA-No Touch NoBụi trong hệ thống quản lý hiện đại.-Thanh toán và duy trì tình trạng của tất cả các máy vàThiết bị. 2008-2010:Sản xuất quản lý / R & D nhân viên tại Hasan Dermapharm AG-Thuận một / Di một khu công nghiệp, Bình Dương, Việt Nam.-Quản lý sản xuất.-Lập kế hoạch cho sản xuất-Đảm bảo mục tiêu-Đảm bảo chất lượng sản phẩm-Đảm bảo làm việc theo với GMP.- Ensure Safety- Ensure Quantity- Ensure On Time- Check out an maintain all machines and equipments- Translate Documents, Preparing, Review, Update SOPs, LogBook...etc.- Familiar with GMP-WHO, GMP-EU.- Cooperate with Planning, Warehouse, QA, QC, EngineeringDepartment...follow with the policy of the company - R&D Staff: Preparing dossier, Translate documents/ dossier forregistration, monitoring design, leaflet, content of box, pakaging...- Research for New Products, new methods, new materials... Education:- Management/Professional of Pharmacy and Science at GADJAH MADAUNIVERSITY, 2005 – 2007 in Indonesia.- Bachelor Science in Pharmacy at GADJAH MADA UNIVERSITY, 1999-2005 in IndonesiaSkills: -Microsoft Office, Internet, Mail.-Leadership Skill.-English, Malaysian, Indonesian, Singaporean, Vietnamese.-Team Works.-5S-Six Sigma-KPI-Lean-EHS-Risk Management-GMP PIC/S-JAPAN – GMP-EU – GMP-WHO - GMP-Etc....Activity:R&D: Research for new products by reference document from books and web to designfor new product, doing the research with lot of Pilot to set up the new formula. Afterstable, do the report to the CEO, coorperate with other department as QA, QC to ensurethe product has pass all of qualification. After that the product will be set up to producewith a production lot and follow up with monitoring the stability of the product with thestress test for 6 months. The sample will be documented and be registered to DAVManufacturing: • Ensure the products are produced according to specifications, work instructions, good manufacturing practices and on time.• Be the workshop leader for optimizing the quality, productivity, and cost reduction;• Making production schedule, directing and controlling the manufacturing activities to ensure adequate supply of stocks;• Balancing the manpower-using planning and production planning per week/month/quarter and year, arrange labour suitable with production plan to ensure high performance of quality and efficiency of machine;• Strictly follow production schedule in order to make things done properly and have best solutions for all problem may happen;• Preparing and approving required documents for production operations, operatortraining requirements, equipment installation, maintenance, etc.. of the production.• Controlling production line during trial run and ramp-up time to ensure all requirements of technical, quality, capacity, delivery are achieved before transfer to Production. Monitoring performances of production line after transfer and implement improvement actions to enhance results.• Setting up goals for production department/staffs and follow up performance progress to achieve final results. • Performing analysis of productivity, equipment capability, operator performanceand implement improving actions to enhance process performances. • Working with Maintenance to perform maintenance activities and also implement preventive maintenance to machinery for downtime reduction and looking for opportunity to improve current equipments, tools for improving production productivity and quality.• Making daily/weekly/monthly production reports for Board of Director.Other:- Establishing and monitoring the effectiveness of quality system, ensure the compliance of GMP requirements- Co-ordinate to propose, implement and review all validation processes; SOPs; - Periodically conduct internal audits in production area, and any related areas in order to verify the compliances of GMP requirements; evaluate and provide corrective and preventive action for any non-compliance or deficiency detected.- Familiar in a quality assurance associate role in a Pharmaceutical GMP manufacture. Have worked in a sterile manufacturing environment.- Familiar in international quality management system standards (Japan GMP – GMP PIC/S) Familiar in validation processes, in setting up quality system according to GMP requirements- English good (writing, reading, speaking skills)- Good computer skills- Good communication.- Working independent or team work.- Be passion, careful and responsible in a working manner.- Leadership Skills
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