Philips

QMS Manager

Posted May 8, 2024
Project ID: PHILJP00026408.1
Location
Eindhoven
Hours/week
40 hrs/week
Payrate range
5435 - 6435 €/month
Application Deadline: May 17, 2024 8:23 AM

Role: Quality Management System (QMS) Manager

Contract: Via Randstad Company

Join our team IP&S and Research as a QMS Manager, a pivotal role responsible for ensuring the maintenance, enforcement, and effective management of a compliant QMS.

Key responsibilities include:

  • Upholding a compliant and effective QMS for Quality and Regulatory (Q&R) processes and Product Quality, guaranteeing adherence to regulatory requirements for medical, non-medical devices, and wellness products.

  • Collaborating with Quality Managers across different organizational domains to establish and uphold the QMS, particularly focusing on Product Development, Launch & Maintenance (PDLM) of innovative products.

  • Establishing transition plans, conducting impact assessments on the existing QMS, setting actionable objectives, and ensuring the application of Quality and Regulatory requirements across all processes.

  • Managing and streamlining internal processes to facilitate seamless communication between QMS and Philips Intellectual Property & Standards (IP&S) and Research, ensuring compliance with evolving Regulations and Standards.

  • Coordinating internal and external audits to sustain QMS compliance and certification to external standards.

  • Implementing robust document control procedures and managing training profiles to ensure efficient training administration.

  • Supporting training administration in accordance with the QMS and contributing to the development of training curriculum as per the Philips Business System.

  • Driving assigned Change Requests to closure as part of the Change Control process.

  • Supporting the deployment of corrective and preventative action processes.

  • Assisting in the execution of the management review process.


Skills & experience required to perform this role:

  • Bachelor’s degree in QA, Engineering or related field with more than 10 years of demonstrated experience in managing QMS within a regulated industry (viz. Medical device, automotive, drugs& Pharma, etc.), preferably in the medical device sector. This includes developing, implementing, and maintaining QMS processes and procedures to ensure compliance with relevant regulations and standards.

  • Experience in driving and managing change within a QMS framework, including assessing impacts, implementing change control processes, and ensuring timely closure of change requests.

  • Manage audit processes, address findings, and implement corrective actions. Experience in Document Control and Training Management:

  • Stakeholder management, excellent communication skills, Strategic thinking


Apply now and let's shape the future of quality together! For any inquiries, reach out to me at Pallavi.mahadik_1@philips.com or via mobile at +31 623460765.

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