Regulatory Affairs Manager

at  Philips

JOB DESCRIPTION

Philips 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

Looking at the challenges the world is facing today Philips’ purpose has never been more relevant. So whatever your role, if you share our passion for helping others, you’ll be working towards creating a better and fairer future for all.

YOU ARE RESPONSIBLE FOR

APAC portfolio

• To formulate and implement the Hospital Patient Monitors (HPM) Businesses and / or Markets long-range regulatory strategies for APAC (Asia Pacific).
• Main point of contact between BU, Market and Local Business Team for product registration preparation and renewals.
• Create regulatory awareness level as determined within the organization.
• Supports implementation of simplified yet robust regulatory processes for registrations and labeling deviations across the HPM Businesses.
• Introduce and implement the necessary regulatory processes and tools required to ensure first time right in submissions.
• Ensure compliance to relevant regulations and other Regulatory Requirements and as required, guidelines and policies to all HPM products and operations are consistent with those regulations.
• Lead the Planning, generation, and coordination of regulatory submissions for HPM product/solution licensing.
• Proactive stakeholder management in BU.
• Define and implement appropriate regulatory certifications for sites. Ensures that all products to be released comply with all the relevant safety and environmental policies and regulations by implementing requirements, conditions, and enablers in the Business and / or Market.
• Formulates and recommends (changes to) policies and establishes procedures that affect immediate organization(s).
• Being part and execute the regulatory compliance guidance and regulatory streamline operational excellence between HPM groups /sites and Markets to ensure time to market on global initiatives especially related to new projects involving Regulatory for key decision makers.
• Develop and maintain, execute and track elicit regulatory requirements as per each country required for regulatory compliance and local regulations and tracking progress of project trackers for the markets impacted against planning, submissions and approvals deadlines

TO SUCCEED IN THIS ROLE, YOU’LL NEED A CUSTOMER-FIRST ATTITUDE AND THE FOLLOWING

• Bachelor’s Degree Holder in related disciplines.
• Minimum 5 years working experience in relevant fields.
• Have dealings with regulatory exposures.
• Ability to present and negotiate effectively in multiple areas of the customers’ environment.
• Excellent in interpersonal and communication skills with proven ability to influence all levels of stakeholders.
• Excellent organizational and time management skills