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Director of Regulatory AI & Digital Innovation

Philips

Director of Regulatory AI & Digital Innovation

full-timePosted: Jan 13, 2026

Job Description

Job Title

Director of Regulatory AI & Digital Innovation

Job Description

Director of Regulatory AI & Digital Innovation:
Role Purpose
Transform IGTS Regulatory Affairs into an AI-powered, digitally enabled function that accelerates speed-to-market, strengthens compliance, and supports innovation in AI, software, and regionally complex markets.

Your role:
Support Regional Regulatory Strategy

  • Shape regulatory frameworks for AI and continuous software delivery; engage early in innovation.
  • Strengthen readiness for NMPA, EU MDR, FDA; ensure digital tooling supports regionalization and dual-track pathways.

Build Future-Ready RA Skills

  • Upskill teams in AI, software regulation, and digital tools; reduce single points of failure; support RA workforce planning.

Drive Cross-Functional Governance

  • Align with Product Management, Portfolio, Advanced Development & Customer Success to embed regulatory strategy across lifecycle.

Lead RA AI Strategy & Tools

  • Deploy structured content authoring, dossier automation, regulatory intelligence curation, and automated QC.

Accelerate Regulatory Execution

  • Reduce manual work, eliminate backlog, and increase global submission efficiency.

You're the right fit if you have:

  • Bachelor's / Master's Degree in (Biomedical) Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent.
  • Minimum 8 years of experience in areas such as Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent.
  • Well versed in AI regulations(NMPA, EU MDR and/or FDA) and how to apply it to Medical devices  Strategic and innovative thinker with a proven capacity to challenge conventions and develop breakthrough solutions.


You are a part of

The global Philips regulatory organization of Image Guided Therapy Systems (IGT-S)  and will be reporting to the Regulatory leader for IGT-S in the Netherlands.  The team you will be working in, is a high-performance, culturally diverse, and very dynamic team. It consists of >50 people working in the areas, divided over China , India and the Netherlands.

How we work together
We believe that we are better together than apart. For this role, this means working in-person at least 3 days per week.


About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• 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 here.

#LI-EU

Locations

  • Best, Noord-Brabant, Netherlands

Salary

Estimated Salary Rangemedium confidence

120,000 - 200,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Regulatory Affairsintermediate
  • Quality Complianceintermediate
  • Product Developmentintermediate
  • AI regulations (NMPA, EU MDR, FDA)intermediate
  • Medical Devicesintermediate
  • strategic thinkingintermediate
  • innovative thinkingintermediate

Required Qualifications

  • Bachelor's / Master's Degree in (Biomedical) Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent (experience)
  • Minimum 8 years of experience in Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent (experience)

Responsibilities

  • Transform Regulatory Affairs into AI-powered function
  • Support Regional Regulatory Strategy
  • Shape regulatory frameworks for AI and software
  • Build RA skills in AI and digital tools
  • Drive Cross-Functional Governance
  • Lead RA AI Strategy & Tools
  • Accelerate Regulatory Execution

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Tags & Categories

Regulatory AffairsQuality ComplianceProduct DevelopmentAI regulations (NMPA, EU MDR, FDA)Medical Devicesstrategic thinkinginnovative thinkingHealthcare Technology
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Philips logo

Director of Regulatory AI & Digital Innovation

Philips

Director of Regulatory AI & Digital Innovation

full-timePosted: Jan 13, 2026

Job Description

Job Title

Director of Regulatory AI & Digital Innovation

Job Description

Director of Regulatory AI & Digital Innovation:
Role Purpose
Transform IGTS Regulatory Affairs into an AI-powered, digitally enabled function that accelerates speed-to-market, strengthens compliance, and supports innovation in AI, software, and regionally complex markets.

Your role:
Support Regional Regulatory Strategy

  • Shape regulatory frameworks for AI and continuous software delivery; engage early in innovation.
  • Strengthen readiness for NMPA, EU MDR, FDA; ensure digital tooling supports regionalization and dual-track pathways.

Build Future-Ready RA Skills

  • Upskill teams in AI, software regulation, and digital tools; reduce single points of failure; support RA workforce planning.

Drive Cross-Functional Governance

  • Align with Product Management, Portfolio, Advanced Development & Customer Success to embed regulatory strategy across lifecycle.

Lead RA AI Strategy & Tools

  • Deploy structured content authoring, dossier automation, regulatory intelligence curation, and automated QC.

Accelerate Regulatory Execution

  • Reduce manual work, eliminate backlog, and increase global submission efficiency.

You're the right fit if you have:

  • Bachelor's / Master's Degree in (Biomedical) Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent.
  • Minimum 8 years of experience in areas such as Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent.
  • Well versed in AI regulations(NMPA, EU MDR and/or FDA) and how to apply it to Medical devices  Strategic and innovative thinker with a proven capacity to challenge conventions and develop breakthrough solutions.


You are a part of

The global Philips regulatory organization of Image Guided Therapy Systems (IGT-S)  and will be reporting to the Regulatory leader for IGT-S in the Netherlands.  The team you will be working in, is a high-performance, culturally diverse, and very dynamic team. It consists of >50 people working in the areas, divided over China , India and the Netherlands.

How we work together
We believe that we are better together than apart. For this role, this means working in-person at least 3 days per week.


About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• 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 here.

#LI-EU

Locations

  • Best, Noord-Brabant, Netherlands

Salary

Estimated Salary Rangemedium confidence

120,000 - 200,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Regulatory Affairsintermediate
  • Quality Complianceintermediate
  • Product Developmentintermediate
  • AI regulations (NMPA, EU MDR, FDA)intermediate
  • Medical Devicesintermediate
  • strategic thinkingintermediate
  • innovative thinkingintermediate

Required Qualifications

  • Bachelor's / Master's Degree in (Biomedical) Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent (experience)
  • Minimum 8 years of experience in Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent (experience)

Responsibilities

  • Transform Regulatory Affairs into AI-powered function
  • Support Regional Regulatory Strategy
  • Shape regulatory frameworks for AI and software
  • Build RA skills in AI and digital tools
  • Drive Cross-Functional Governance
  • Lead RA AI Strategy & Tools
  • Accelerate Regulatory Execution

Target Your Resume for "Director of Regulatory AI & Digital Innovation" , Philips

Get personalized recommendations to optimize your resume specifically for Director of Regulatory AI & Digital Innovation. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Director of Regulatory AI & Digital Innovation" , Philips

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

Regulatory AffairsQuality ComplianceProduct DevelopmentAI regulations (NMPA, EU MDR, FDA)Medical Devicesstrategic thinkinginnovative thinkingHealthcare Technology
Quiz Challenge

Answer 10 quick questions to check your fit for Director of Regulatory AI & Digital Innovation @ Philips.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.