.**Job Title**: Regulatory Affairs SpecialistPhilips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow.But it's not just what we do, it's who we are. We are 80,000, wonderfully unique individuals, with two things in common. An unwavering sense of purpose and a relentless determination to deliver on our customers' needs. It's what inspires us to create meaningful solutions - the kind that make a real difference - when it matters most.The world and our customers' needs are changing faster than ever before and while we are proud of what we do already, we know we can do more. That's why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs.**In this role, you have the opportunity to make life better**Guide & support Businesses, Markets and supporting functions of regulatory needs of the Mexico market for medical and non-medical products/solutions under your responsibility including the development of regulatory strategies for new and existing products/solutions, execution of regulatory submissions and engagement with external associations.**You are responsible for**- Communicating on time and accurate Mexico specific regulatory requirements and advise business partners/product design teams of regulatory strategy and requirements- Implementing global regulatory strategies and roadmaps through understanding competitive market landscape and product marketing strategies- Preparing regulatory submissions for new products/solutions, product changes, and re-registrations as required for Mexico and LATAM countries.- Planning and maintain registration information and obtain re-registration approvals in advance of license expirations to ensure no disruption in product availability.- Maintaining and organizing appropriate regulatory records to demonstrate compliance with applicable regulations in Mexico and LATAM.- Supporting development of regulatory plans, risk assessments and required activities to meet regulatory requirements and product registrations to maintain compliance- Acting as advisor cross- functionally to meet the schedules and/or solve technical questions**You are a part of**The Regulatory Affairs team of Latin America, where you will influence and lead the Regulatory Affairs efforts with the business.**To succeed in this role, you'll need a customer-first attitude and the following**- Ability to work in a matrix organization with multiple stakeholders internal and external to ensure time to market