Philips

Technical Complaint Investigation Specialist

Posted Jun 24, 2025
Project ID: PHIAJP00002425
Location
Best
Hours/week
40 hrs/week
Timeline
11 months , 4 weeks
Starts: Aug 1, 2025
Ends: Aug 1, 2026
Payrate range
4000 - 5800 €/month
Application Deadline: Jun 27, 2025 12:00 PM

Join Philips to ensure patient safety and product excellence by leading in-depth complaint investigations for high-risk medical devices. Your work will directly impact product quality and regulatory compliance across the globe.

Your role:

As a Technical Complaint Investigation Specialist, you’ll play a key role in Philips’ Quality & Regulatory organization. You'll focus on root cause analysis of high-risk complaints, supporting technical investigations, vigilance reporting, and product improvements. By working closely with R&D, Manufacturing, Clinical, and Regulatory teams, you’ll help drive continuous improvement in our healthcare solutions.

You're the right fit if you have:

  • A Bachelor’s or Master’s degree in Engineering or Science

  • 7+ years of experience in a regulated medical device industry, ideally in R&D and/or Quality

  • Strong understanding of complaint handling, adverse event reporting, and post-market surveillance

  • Knowledge of regulatory standards (21 CFR Parts 803, 806, 820, ISO 13485, ISO 14971, EU MDD, Canadian MDR, MHLW 169)

  • Experience within Philips Healthcare is a plus

  • A passion for product improvement, quality, and patient safety

  • Excellent communication, analytical, and stakeholder collaboration skills


What you’ll do:

  • Lead technical investigations of high-risk complaints and customer feedback

  • Develop and apply investigation strategies and guidelines, including use of AI/LLM tools

  • Collaborate with R&D, Clinical, Sustaining Engineering, and Manufacturing

  • Support failed parts return process, complaint triage, and product defect reviews

  • Engage with global regulatory bodies and support audits and inquiries

  • Contribute to CAPAs, Corrections & Removals (C&R), and training programs

  • Identify complaint patterns and drive systemic improvements

  • Represent the business in cross-functional quality activities


Practical Info:

  • Must reside in the Netherlands

  • Contract type: Work at Philips through Randstad, with access to employee benefits


Why join Philips?

  • Impactful work: Help ensure the safety and quality of life-saving devices

  • Cross-functional collaboration: Work with top experts in Quality and R&D

  • Culture of innovation: Use cutting-edge tools and methodologies

  • Growth opportunities: Advance in a global health tech leader with a purpose

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