东莞招聘

职位描述：

Job Description Summary:
1. Ensures the annual definition of the quality improvement plan (QIP) based on business needs and timely implementation.
2. Supports on-site/off-site supplier quality development including coordination /management of required internal/external resources.
3. Manages the early involvement of suppliers in new product development and product/component improvement. Leads quality system audits.
4. Deploys and follows-up on the Supplier Quality Related KPI’s towards the supplier.
5. Ensures the assigned supply base meets the Philips sustainability requirements. Ensures the timely and correct GSRS data-input. Participates in the Supplier Selection process for the quality aspects.
6. Defines supplier quality requirements for new / improved products ensuring all. manufacturability aspects at suppliers (improve supplied quality).

Description:

Independently Produces and completes Supplier Quality Engineering related activities and documentation.

Completes Qualification of materials and components (including spare parts), development/ improvement of supplier processes for CtQ's, supplier process control plans; ensuring that the supplied part meets specifications, and the control limits/tolerances for CtQ parameters are met.

Qualifies and sustains sub-processes of suppliers, including performing process validations for critical supplier processes impacting part quality.

Ensures that the components/products at the supplier (including spare parts and services) are released according agreed specification and quality requirements (APQP / PPAP), and SQ audit results.

Executes SCAR management, ensuring effective and timely closure.

Independently works to deploy common approaches and working methods to drive ‘’One Philips’’ towards Supply Base in the assigned BG or Market.

Works on issues of diverse scope where analysis of situation or data requires identification and evaluation of a variety of factors, including an understanding of current business trends.

Follows processes and operational policies in selecting methods and techniques for obtaining solutions.

REQUIREMENTS:

Education:

• Bachelor’s degree in an engineering or science discipline, or equivalent experience.
• Current certification with a recognized Accreditation body (i.e., RAB-QSA/IRCA) or successful completion of ASQ certification as a Certified Quality Engineer (CQE) and Certified Quality Auditor (CQA) or Certified Biomedical Auditor or successful completion of a recognized Lead
  

Experience and Background:

• At least 8yrs above work experience in Quality Function, Good knowledge of Plastics Injection Molding processes or Packaging manufacturing technologies. Experience in Medical industry is a plus.
• Good written and oral English skills.
• Experience in root cause analysis, corrective and preventive action methods.
• Expertise/experience in problem solving with quality tools such as: 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc.
• Good knowledge of production/quality development and control methods; CtQ definition, DfSS, SPC, APQP, FMEA, Control Plans, etc.)
  

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