陈利芳

陈利芳 Email and Phone Number

Quality Manager @ Maccura Biotechnology
chengdu, sichuan, china
陈利芳's Location
Chengdu, Sichuan, China, China
About 陈利芳

In terms of profession, Over 14 years work experience in quality, 11 years quality team management experience, and rich experience on project management. Good at quality control tools and product quality control planning.Have rich experience on project management, supplier management, new product introduction quality control, parts quality control, especially for selection, sourcing, assessment and management of suppliers.Have good knowledge of different electrical components and mechanical components, such as LCD/display, inverter, connector, cables, mechanism etc. Good knowledge on MRI/CT/Ultrosound/DR.Certificate on ISO 9001/ISO13485 as internal auditor. Intermediate quality engineer certificated. Good command of SPC、FMEA、GR&R, 8D, QC 7 tools, familiar with TS 16949,ISO 14000, 6 sigma、Reliability technology and so on.As for characteristic, outstanding multi-industry adaptability, quick learner with strong learning ability, great executive power. Excellent in driving supplier and project management. Good ability on communication, organization, problem solving.

陈利芳's Current Company Details
Maccura Biotechnology

Maccura Biotechnology

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Quality Manager
chengdu, sichuan, china
Employees:
31
陈利芳 Work Experience Details
  • Maccura Biotechnology
    Quality Manager
    Maccura Biotechnology Jan 2019 - Present
    Chengdu, Sichuan, China
    management representative and quality manager.in charge of quality control and quality system.
  • Alltech Medical System
    Quality Control Manager
    Alltech Medical System Mar 2011 - Dec 2018
    Chengdu
    1. Supplier management: plan for supplier management procedure, define the criteria of selection/sourcing/qualification of new supplier, release the checklist of supplier survey and annual assessment. Lead SQEs to optimize the management method, identify weak points of supplier manufacture process, increase the process capacity, continuously improve product quality and make sure deliverability. 2. Product quality planning: plan for the product monitoring and measurement. Define control processes of monitoring and measurement, from incoming quality control, process quality control, final quality control, outgoing quality control, to on-site installation & acceptance. 3 Parts quality control: update the sampling plan, lead IQC to find out the key items for quality control, follow the issues during new product phase in, push supplier to improve and drive the engineering Dept. to change the specification and drawings in case of need. 4. Supplier change control: define the procedure of supplier change approval, including scope and verification requirements, organize review and release.6. Quality system management: organize the internal audit and 3rd party audit and management review. Organized many times of process review in a particular period.5. New product development control: participate in new product introduction management and phase review, control and assure the quality of new product, among the stages of project directive, development, verification and validation, pilot production, design transfer, mass production, marketing, service.6. ECR/ECO control: worked as project manager to control the engineering change request and change order, make sure all changes are verified sufficient and released/implemented according to the rules. 7. Project management: New product Breast dedicated MRI system management. including project management and DHF document preparation as well as CFDA registration.
  • Quanta Shanghai Manufacture City(Qsmc )
    Supplier Quality Specialist
    Quanta Shanghai Manufacture City(Qsmc ) Jul 2007 - Feb 2011
    Shanghai
    In charge of supplier quality control concentrate on LCD & inverter of Apple I-mac & Macbook.1. Implement new supplier survey and annual audit for the suppliers in AVL. Using QSA,QPA,GP checklist based on ISO9000&14000,OHSAS18000,SA8000.2. Conduct on-site following in supplier side during qualification stage, validate new production line, including re-optimize before build start, readiness check, process risk assessment, SPC control, outgoing inspection, field rate for production line, dimensional data(FAI, Cp/cpk) , electrical parameter data as well as following FMEA...3. Solve material issues during the whole qualification stage of new products. Study with customer & suppliers for any known/potential quality or design issues to make sure mass production go through smoothly. 4. Deal with mass production material quality issues, review 8D&CLCA&FA reports, follow up the corrective actions, track on-site in case of need, confirm the effectiveness till completion.5. Perform supplier general management: by gathering and sorting quality data from production line and vendors, monitor the performance of vendor’s quality, hold regularly supplier meeting or QBR meeting with supplier and customer, on-site audit in case of need.6. Handle and approve ECR&ECN applied by suppliers: co-work with the related teams to evaluate and give approval.7. Push and train all related guys (IQC& Product Engineer & Vendors) to have Spec known clearly, to make inspection procedure /method /tools standardized & correlated. To make sure the consistency of inspection results from different stations.8. Deal with GP issues (mainly for RoHS & HF non-conformity).Follow up the effectiveness of GP control process and optimize it. On-site audit in case of need.
  • Tpv Display Technology(Wuhan)Co.,Ltd
    Supplier Quality Supervisor
    Tpv Display Technology(Wuhan)Co.,Ltd Jul 2004 - Jun 2007
    Wuhan
    Responsible for the management of electronic components’ SQE/IQC team.1. Deal with material quality issues and quality risk assessment, cooperate with customers and suppliers in the root cause analysis and corrective action, and track the effectiveness.2. Source and certificate new suppliers, audit and evaluate suppliers in AVL routinely, ensure the quality of finish product3. Confirm the targets of department (KPI), and ensure the achievement of the targets with quality control tools.4. Confirm the SOP of IQC inspection, and ensure the parts quality.5. Define the requirement of component development according to quality status, put forward proposals for component design, and follow-up the parts qualification procedure.6. Cooperate with purchaser in competitive bidding of suppliers, to achieve the targets of cost down 7. Participate in internal audit, and receive OEM-customer’s audit.

陈利芳 Education Details

Frequently Asked Questions about 陈利芳

What company does 陈利芳 work for?

陈利芳 works for Maccura Biotechnology

What is 陈利芳's role at the current company?

陈利芳's current role is Quality Manager.

What schools did 陈利芳 attend?

陈利芳 attended Sichuan University, Jianghan University.

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