Philips

QMS Manager

Posted Mar 18, 2020
Project ID: PHILJP00021644
Location
Best , Brabant
Duration
11 months, 4 weeks (Apr 1, 2020 - Apr 1, 2021)
Hours/week
40 hrs/week
Payrate range
36 - 62 €/hr

In this role, you have the opportunity to be part of the dedicated Quality team for Factory Best. As QMS manager you will be reporting into the PQMS Q&R function and will have a dotted line to the Quality leader of Factory Best. The Quality team of factory Best focusses on ensuring product quality, while maintaining full compliancy and driving manufacturing excellence. The aim is to achieve timely releases of products with high quality and outstanding reliability.


By joining this organization, you will be part of the transformation journey towards a world class Operations organization to better serve our customers with speed and excellence.


As a QMS manager you have the opportunity to be at the heart of establishing and maintaining the Quality management system for the Factory Best organization.

You are responsible for

  •  Ensuring compliant and effective Quality Management System (QMS) is maintained.
  •  Accountable for the transformation of all current QMS parts in scope towards the single Philips QMS (PQMS) structure.
  • Managing (local) Q&R processes and ensuring (local) process ownership for all activities under the PQMS governance in scope.
  • Ensuring Q&R requirements are effective in all processes in scope.
  • Maintaining, enforcing, and managing a compliant and effective QMS for the activities in scope.
  • Managing the transition/deployment of the PQMS.
  • Ensuring the addition and management of any local QMS documents in line with the evolution of the PEPF and the PQMS.
  • Facilitating and driving the management review within Factory Best.
  • Ensuring training and training registration as per the QMS.


You are a part of the Quality team of Factory Best, which is one of the main Operation sites for Health Systems within Philips. Factory Best team is driving operational excellence and manufactures, refurbishes and repairs our medical devices & components in a safe, compliant, and effective manner.

Requirements

•   Quality Systems Management knowledge and common standards and regulations

•   Demonstrated ability to understand and develop processes.

•   A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways.

•   Frequently interacting with subordinate supervisors, customers, and/or functional peer group managers, normally involving matters between functional areas, other company divisions or units, or customers and the company. Often must lead a cooperative effort among members of a project team.

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

•   Minimum of three years of similar work experience.

•   Experience working in disciplined regulated industry.

•   Demonstrated ability to interact and communicate in Dutch and English, including demonstrable writing, speaking, and comprehension skills; ability to communicate across levels of the organization.

•   Strongly preferred: proven experience in multi-site, multi-disciplinary quality organizations

•   Character: people-oriented, no-nonsense, pro-active, make-it-happen mentality, pressure-resistant, hands on, able to get things done from people, disciplined

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