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Taking corrective and preventive action within the functional scope of his/her dept。 Responsible for the pleteness and correctives of quality records in his/her dept。 OnJob training to staff of his/her dept/section。 The implementation of quality policy and quality system in his/her dept/section。 Controlling of puter network documents amp。 Assuring appropriately use of puter and relevant software。 Designing, installment and maintaining to hardware and software system to each dept/section。 Providing and managing resources needed such as water, power and gas resources178。178。 Maintaining the delivery vehicles.F Purchasing Manager 178。 Responsible for all production delivery and transportation。178。178。178。 Responsible for normal operation of store dept., shipping dept., custom declaration dept. and purchasing dept.F Store Manager 178。 Assuring the clean of the workspaces。178。 F Administration manager178。 178。178。178。178。178。 Assist with pricing strategies for the key customers, and maximize margin opportunities. F Human resource manager178。 Introduce the innovative technology and conceptions with manufacturing process to advance pany’s engineering strength and petitive advantage。 Ensure and monitor the performance of continuous improvement program in production flow to enhance the products quality and production efficiency。 Monitor the quality and delivery schedule to meet the customers’ requirements。 Ensure that all pany operating procedures and controls are applied。 Select, train, develop and motivate staff in accordance with pany procedures and ensure that all their activities meet the standards required。 Report to General Manager, responsible for the day to day operation of the departments which include Production, PPC, Facility, Facility Engineering, to maximize business growth and profitability, setting clear objectives and targets for above 。178。178。178。178。178。178。 Cooperate well with the internal departments/sections and handle all the problems timely。178。 Responsible to the routine of manufacturing Engineering Department。178。 Responsible for the application of statistical techniques amp。 Responsible for control of document and Data。 Handling of nonconforming product and convening MRB meeting。 Arranging the measurement work of trial run product and inprocess product,178。 Executing the quality control of product,178。178。167。167。167。 Organizing to establish and maintain ISO9001 Quality management system, including:167。178。178。178。178。178。178。178。 Managing the operation of the program management department, manufacturing Engineering department and the tooling repairing amp。 under his control systems amp。 Promoting awareness of customer requirements throughout the organization.F Director of Finance / Senior Member of the Management Team178。 Ensuring that a quality management system is established, implemented and maintained in accordance with the ISO9001:2008 Standards.178。178。 Handling serious customer plaints, entertaining customer visitor amp。 Approving quality manual and quality procedure。 target together。 Improve business operation process178。 Strategic planning。 marketing activities。178。178。 Ensuring quality objective amp。178。178。178。 authority of each FP employee are defined and approved by the manager or superior of each position in every department. (b) Job Description Form stipulates the main work responsibility of each employee and it is the responsibility of each dept head to ensure that the Job Description is generated and properly understood by all his/her subordinated staff, meanwhile, to check if his/her subordinated staff have fulfilled his/her responsibility.III The responsibility and authority of senior management and all departmental managers:F General Manager: Responsible for the pany quality management system:178。 measurement methods FQPQIP02F Our quality objectives and targets are measurable and consistent with our quality policy as well as including those needed to meet requirements for product. Quality Management System planningF In order to meet the requirements of quality objectives amp。 Data Control” (FQPDOC01) to manage the documents of quality management system to ensure:(a) To approve documents for adequacy prior to issue (including update)(b) To ensure that documents remain legible and readily identifiable and ensure the current revision status are identified,(c) To ensure that relevant versions of applicable documents are available at points of use,(d) To prevent the unintended use of obsolete documents through removing them from all points of issue and use, (e) To apply suitable identification to them such as with stamps of “Obsolete” or “Valid before“ on them if the obsolete documents are retained for any purpose.(f) Ensure the external documents and data are marked and their distribution is controlled.(g) Control all customersupplied documents and data. Control of recordsWe establish procedure Quality Record Control (FQPDOC02) to control the following:(a) Each dept manager or section supervisor is responsible for working out the forms of quality records and their review. (b) All quality records must be filled with truth, details and pleteness. Data must be accurate and reliable and readily identifiable.(c) All the quality records must be collected, indexed, filed and stored.(d) Quality records shall be stored and retained in such a way that they are readily retrievable, it is also required to provide a suitable environment to prevent damage, deterioration or lost.(e) Staff looking up quality records must be approved by the dept that preserves the records. While the outsider’s looking up must be approved by preserving dept manager/supervisor. Quality records shall be available to the customer if required in the contract. (f) The retention time and disposition of recordsApplicable procedures: FQPDOC01 Document and Data Control