Quality Management System (QMS) Specialist at Philips
Best, , Netherlands -
Full Time


Start Date

Immediate

Expiry Date

03 Dec, 25

Salary

0.0

Posted On

04 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

JOB DESCRIPTION

The Quality Management System (QMS) Specialist is part of the dedicated Quality team for the multi-modality factory, Factory Best. The Quality department ensures product quality, while maintaining full compliancy and driving manufacturing excellence to achieve timely releases of products with high quality and outstanding reliability. As a QMS specialist you will work in the QMS team who maintains the QMS, manages internal and external audits and manages CAPA.

Responsibilities
  • Assists the Factory Best organization by managing and taking ownership of local Q&R processes, addressing compliance deficiencies and ensuring local process ownership for all activities under the QMS governance in the assigned areas (Audits, Document Control, Training, CAPA) to ensure that the QMS is efficient and meets the regulatory requirements.
  • Contributes to the development, implementation, and revision of QMS processes and quality manuals, ensuring their accuracy, clarity, and compliance with relevant standards. Participates in continuous improvement initiatives within the QMS, proposing and implementing enhancements to processes, tools, and systems to drive overall quality performance and operational excellence. Check QMS document changes for compliance and effectiveness, e.g. ISO13485.
  • Contribute to the availability of metrics/KPI data to measure training effectiveness, PQMS deployment and QMS compliance.
  • Prepares for and participates in external regulatory audits and inspections by ensuring readiness of documentation, processes, and records, and provide responses to audit findings in collaboration with stakeholders. Ensure proper audit planning and schedule meets the requirements of internal and external policies and external regulations.
  • Support Business Units with regulatory submissions, for new products/solutions, existing products/solutions. Support training and training administration as per the QMS and contribute to training content for local QMS documents as necessary.
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