Philips, the global leader in health technology and electronics, is currently recruiting a Regulatory Affairs Specialist to join its expanding team in Eindhoven, Netherlands. The role supports product registrations and compliance across the EU and international markets.
This opportunity is open to both EU and non-EU candidates, with visa sponsorship options available for exceptional international professionals in health tech and compliance.
📌 Job Overview
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Job Title: Regulatory Affairs Specialist
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Company: Philips
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Location: Eindhoven, Netherlands
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Job Type: Full-Time (Hybrid)
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Field: Medical Devices / Health Technology
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Experience Level: Mid-career
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Application Deadline: Open (rolling recruitment, July 2025 intake)
🎯 Key Responsibilities
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Coordinate product registrations and regulatory filings in the EU and other target markets
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Interpret medical device regulations (MDR, ISO 13485, FDA, etc.) and apply them to product portfolios
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Communicate with government authorities and Notified Bodies
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Ensure product documentation, clinical evaluations, and quality systems comply with local/international regulations
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Support audit readiness and internal training on compliance topics
👤 Requirements
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Bachelor’s or Master’s degree in Biomedical Engineering, Pharmacy, Life Sciences, or a related field
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Minimum of 3–5 years’ experience in regulatory affairs, preferably in medical devices or healthcare
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Good knowledge of EU Medical Device Regulation (MDR)
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Experience with international submissions (e.g. FDA, China NMPA, Health Canada) is an advantage
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Strong communication, documentation, and organizational skills
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Fluent in English; Dutch is a plus, but not mandatory
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Visa sponsorship may be provided for qualified candidates outside the EU
💼 Benefits
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Competitive salary based on experience
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Hybrid work model with flexible hours
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Relocation support and work visa sponsorship (where applicable)
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Pension scheme, bonus, and wellness programs
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Global exposure through a multinational team and projects
📨 How to Apply
Apply through the official Philips careers portal:
👉 https://www.careers.philips.com
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Use the search bar: “Regulatory Affairs Specialist – Netherlands”
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Choose the Eindhoven posting and complete the application form
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Attach an updated international CV and motivation letter clearly stating regulatory experience
📢 Tip: Tailor your CV to highlight regulatory documentation, MDR readiness, and any international product launch experience. Mention any audit or compliance systems you’ve worked with.