We are seeking a highly skilled and motivated engineer who is passionate about Project controller and executor that ensuring the projects is meet the timeline. Participate in developing the protocol and the report of method validation, verification, and transfer activities. Conduct testing using analytical instruments such as HPLC, AAS, GC, UV-Vis spectrophotometer, and dissolution apparatus related to the project. Prepare and review analytical reports and documentation in compliance with GMP and regulatory requirements. Ensure laboratory activities comply with SOPs, GLP, and GMP standards. Handle out-of-specification (OOS) investigations and deviation reports. Maintain laboratory instruments, calibration, and documentation. Support internal and external audits.
We are seeking a highly skilled and motivated employee who is passionate about Manage production projects for pharmaceutical and food & beverage production lines. Oversee and review batch production records to ensure accuracy and compliance. Translate the master production schedule into daily shift production tasks. Monitor process parameters to optimize yield, reduce waste, and improve production efficiency. Perform validation and qualification of production machinery. Allocate manpower effectively to ensure smooth operations and minimize downtime. Ensure compliance with GMP, Myanmar FDA regulations, and internal company standards. Coordinate with quality assurance and maintenance teams to resolve production issues.
We are seeking a highly skilled and motivated engineer who is passionate about Make schedule and monitoring implementing the condition of the machine production, Utility and Calibration equipment being maintained regularly. Ensure Perform preventive maintenance work on utilities / building facilities according to schedule Ensure Perform corrective work on utility units, and building facilities according to the Work Order (WO) of all departments Reporting all activities that have been carried out in the form of realization of daily work reports and conveying critical information Handle Spare part Management dan Monitoring
We are seeking a highly skilled and motivated engineer who is passionate about Maintain and improve the Pharmaceutical Quality Management System (QMS) Control and manage documentation (SOPs, Working Instruction, forms, specifications, master documents) Handle deviation, CAPA, change control, and risk management processes Coordinate internal audits and support external audits (regulatory & customer audits) Ensure compliance with GMP, GDP, GLP, and company policies Conduct training on quality systems and GMP requirements Support product complaints and recall procedures when required Prepare quality metrics and management review reports Handle qualification document and executing of qualification of the facilities, machines and instrument.
Provide support for networking administration. Define privacy and information security policy. Keeping inventory of hardware and maintenance records Oversee network and server Provide IT Audit semester report Overseeing computer security and antivirus updates etc. Timely respond to user inquiries via email, chats, over the phone or in person Software installation, configuration, user onboarding/deboarding related functions CCTV, Door Access and other related IT devices Diagnosis and resolve the Hardware, Software and Network connectivity trouble shooting Purchase Requisition for IT related products, services & peripherals Relevant Process preparation as and when needed Validate and ensure necessary information security measures to be in place Other necessary tasks assigned by IT HO team
We are seeking a highly skilled and motivated engineer who is passionate about Monitoring and Operating Utility Machine Preventive Maintenance Production Machine Conduction small project Work Order Implementation
Daily Factory Operations: Based on-site at the manufacturing facility to oversee and ensure all daily production activities align with regulatory standards. National Compliance & Coordination: Act as the primary liaison with the Myanmar Food and Drug Administration (FDA) and other local authorities to manage product registrations, renewals, and variations. Product Lifecycle Management: Lead the submission and tracking of regulatory dossiers for new product registrations and ensure timely updates for any product variations based on company needs. International Regulatory Alignment: Coordinate with external regulatory bodies and head office organizations to ensure compliance with international standards for exported products . Cross-Border Collaboration: Work closely with the global head office to harmonize local regulatory strategies with international requirements and corporate policies. Regulatory Intelligence: Stay updated on changes in both domestic and international pharmaceutical laws to ensure the factory remains in full compliance at all times.
Sourcing & Vendor Management (ပစ္စည်းများရှာဖွေခြင်း နှင့် Supplier များနှင့် ဆက်သွယ်ဆောင်ရွက်ခြင်း) Purchasing & PO Administration (ပစ္စည်းများဝယ်ယူခြင်းနှင့် အမှာစာ လုပ်ငန်းစဉ်များစီမံဆောင်ရွက်ခြင်း ) Logistics & Customs Compliance (သယ်ယူပို့ဆောင်ရေးနှင့် အကောက်ခွန်ဆိုင်ရာ လုပ်ငန်းစဉ်များစီမံဆောင်ရွက်ခြင်း) Production Planning & Forecasting (ထုတ်လုပ်မှု အစီအစဉ်ရေးဆွဲခြင်းနှင့် ကြိုတင်ခန့်မှန်းတွက်ချက်ခြင်း) Inventory & Materials Control (ကုန်ပစ္စည်းလက်ကျန်နှင့် ကုန်ကြမ်းပစ္စည်းများ ထိန်းချုပ်ဆောင်ရွက်ခြင်း) Supply Chain Coordination (Supply Chain နှင့်ဆကိနွယ်သောလုပ်ငန်းစဉ်များ ချိတ်ဆက်ညှိနှိုင်းဆောင်ရွက်ခြင်း)
We are seeking a highly skilled and motivated employee who is passionate about Analysis and stability study finished porducts Preparation of analytical reports Perform analysis for starting material and finished product Doing administration Job