Let us start with pin pointing some of the must have experience for this position:
- Medical Device Experience,
- Supplier Quality Experience.
In this role, you have the opportunity to implement and manage Quality Engineering, Purchasing Controls and Supplier Quality processes related to the development, procurement and continuous improvement of manufacturing materials, components, software, sub-assemblies, contract manufactured finished devices/products or services, and their introduction into Philips supply chain
You are responsible for
o Collaborating with R&D, Operations and Procurement personnel to proactively engineer quality and ensure compliance for raw materials, components, finished products etc., from suppliers.
o Developing and supporting regulatory compliance gaps at suppliers, including supplier quality system and process development activities.
o Managing the quality relationship with key suppliers.
o Owning and managing the systems, which directly measure, and control in- bound quality and compliance including Material/ Component Specification Standards, Supplied Material Risk Rating, Supplier Risk Rating, and Supplier Rating/Response.
o Ensuring quality conformity of supplies via active monitoring of the supplier performance and take corrective actions (incident, complaint handling), including supplier audits and follow up on system failures.
o Driving quality and compliance development and/or improvement at suppliers when needed; Philips face to supplier(s) on lean improvements.
o Ensuring compliance to regulatory requirements and procedures for regulated products/processes.
o Independently works to deploy common approaches and working methods to drive ‘’One Philips’’ towards Supply Base in the assigned BG or Market.