Responsible for ensuring that the products meet the delivery target with the standards of quality, efficiency, and safety.
Review production plan to identify risks and communicate to management team.
Plan inventory management technique to avoid any shortages and excesses.
Track production schedules and make sure that are met by communicating changes to the production team.
Prepare reports on the status of production, including any delays or problems that may occur.
Review production reports to identify any potential problems with the product.
Coordinate with various departments, such as production, engineering, quality control and quality assurance to plan and manage production activities. And monitor and analyze production data, identify and resolve any issues, and prepare reports on the status and performance of production.
2
Regulatory Affairs Engineer
แผนก: Regulatory Affairs
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เปิดรับจนกว่า Headcount ครบตามแผน
Resume
Proper Picture
Copy of Identification Card
Copy of Education Certificate
Copy of House Registration (optional)
รายละเอียด : Regulatory Affairs Engineer
Assist in establishing and maintaining regulatory functions and systems to ensure continuous medical device and environmental regulatory compliance.
Register new products with the appropriate agencies and organizations and maintain the registrations of existing products according to the applicable regulatory strategies.
Provide guidance to the Engineering staff on the creation and maintenance of Design History Files (DHF), Device Master Records (DMR) and Technical Files.
Define and document corporate regulatory practices within the Quality Management System to maintain compliance with applicable regulatory agencies.
Adhere to and promote all organizational policies and procedures.
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