Regulatory Affairs Specialist
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Position Overview & Specifications
Job Title
Regulatory Affairs SpecialistJob Description
Help bring to market innovative and advanced monitoring, cardiac therapy and data management solutions for pre-hospital customers.
Your role:
Innovation matters when providing medical devices to those working in Emergency Care. As a Regulatory Affairs Specialist you will directly support registration and licensing of new and evolving devices that will make a difference across the US, Canada, and EU.
In this highly collaborative role, you’ll share your knowledge of regulatory principles, theories, and concepts with multidisciplinary teams to guide on risk management, support technical documentation files and prepare regulatory documentation.
This role offers you chance for hybrid working from our vibrant & exciting new offices in Farnborough, Hampshire.
From competitive salary and performance bonus to family friendly policies, flexible benefits and access to Philips University, a career at Philips comes with all sorts of wonderful benefits. Be sure to speak to your recruiter about all the benefits on offer.
You’re the right fit if:
You interested in developing a Regulatory Affairs career within the medical device industry and can demonstrate some knowledge of medical device regulations (21CFR), FDA law, MDD/MDR, other global laws and regulations.
You have a related Bachelors degree ideally within Biomedical Engineering or the Sciences, although we will consider all combinations of education and experience.
You’re an excellent communicator with experience of working with cross functional teams to achieve a common goal.
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 commitment to diversity and inclusion here .
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 here
Discover our rich and exciting history here
Learn more about our purpose here
About Philips UKI
In the UK, we are recognised as a Disability Confident employer and are proud to be part of the Armed Forces Covenant & Mental Health at Work Commitment. We welcome all applicants including those from minority backgrounds, LGBTQIA+ and individuals living with a disability.
Because we are at our best when you are, you can safely share any reasonable tools or adjustments needed during our recruitment process and beyond.
For more information, read our Inclusion and Diversity Policy and, to know more about your Human Rights, we encourage you to view this report.
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Candidate Selection & Onboarding Process
Application & Resume Screening
Submit your tailored CV/Resume directly to the talent acquisition portal.
Technical & Competency Interviews
Virtual interviews with the hiring manager and multidisciplinary team.
Formal Offer & Benefits Negotiation
Written agreement outlining compensation, equity, retirement vesting, and relocation allowances.
Onboarding & Corporate Integration
Equipment provisioning, team orientation, and commencement of duties.
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Regulatory Affairs Specialist • Philips
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