~47m ago
New

Compliance and Quality Specialist (CAPA)

2 Locationsmid
Manufacturing & ProductionQuality Manager
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Quick Summary

Key Responsibilities

In this role,

Requirements Summary

Bachelor’s Degree in Any Science Degree (Physics, Chemistry, Biology, etc.), Engineering (with or w/o license), Health and Safety, Medical Technology,

Technical Tools
Manufacturing & ProductionQuality Manager
Compliance and Quality Specialist (CAPA)

The Compliance Quality Engineering Team of the Quality Enterprise Services organization of Philips manages the quality engineering processes of the commercial operations including quality nonconforming investigations, equipment calibration issues, out-of-tolerance cases, and investigations of other nonconformities to support compliance, continuous improvement, patient safety, quality, and maintain our license to operate.

Responsibilities

~1 min read

  • →In this role, the person will lead a group of individuals in the analysis of defects to determine dispositions of non-conformances and manage non-conformances
  • →Facilitate effective Corrective and Preventive Actions (CAPA) as well as support continuous improvement within the Quality Management System (QMS).
  • →Propose and implement enhancements to processes, tools, and systems as well as build strong relationships with internal and external partners
  • →Drive overall quality performance and operational excellence to ensure regulatory compliance through improvement initiatives
  • →This person will be supporting Asia Pacific - ANZ, Philippines, Vietnam, Thailand, Malaysia, and Indonesia (and other countries as needed by the business)

Requirements

~1 min read
  • Bachelor’s Degree in Any Science Degree (Physics, Chemistry, Biology, etc.), Engineering (with or w/o license), Health and Safety, Medical Technology, Pharmacy and/or Biomedical Engineering
  • Minimum 3+ years working experience in Quality Assurance, Quality Control, Regulatory Affairs, CAPA, Supplier Quality and/or Risk Management
  • Medical devices and/or pharmaceuticals experience is preferred but individuals from the automotive industry are welcome to apply
  • Basic understanding of CAPA, as well as global medical device or pharmaceutical regulations, requirements; and standards such as ISO 13485, ISO 9001 and ISO 14971 (optional) is advantageous
  • FDA experience is advantageous
  • Excellent Communication Skills both in word and writing
  • Strong Business understanding and ability to work independently and under pressure
  • Highly Flexible in terms of work schedule
  • Strong Stakeholder Management and Great Team Player
  • Advance knowledge in Microsoft programs (Excel, PowerPoint, etc.)


Are you ready to do the work of your life to help the lives of others? Learn more about our business, discover our rich and exciting history and learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care.

Location & Eligibility

Where is the job
Not specified
Location terms not specified
Who can apply
Same as job location

About this job

Posted
Today
Employer
has 781 open jobs on Jobera in 34 countries.

Listing Details

First seen
October 25, 2026
Last seen
October 25, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
49%
Scored at
October 25, 2026

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Compliance and Quality Specialist (CAPA)