Regulatory Affairs Manager, Hospital Patient Monitoring META
Location Riyadh, Ar Riyad, Saudi Arabia Job Type Full time Job Id 521457 Posted Date: 04/26/2024 JOB DESCRIPTION
Job Title
Regulatory Affairs Manager, Hospital Patient Monitoring META
Job Description
Job title:
Main point of contact between BU, Market and Local Business Team for product registration preparation and renewals.
You are responsible for
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
You're the right fit if:
Education: Bachelor’s degree.
•Experience: At least preferably 6 years of Regulatory Affairs experience in medical industries or pharma sectors.
•Excellent command of English and Arabic is required.
•Be familiar with ISO 13485, ISO 9001 ,MDD 93/42/EEC or EU-MDR.
•Excellent organization and coordination skills.
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.
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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 .
Over 125 years ago, Frederik and Gerard Philips started a small light bulb company in Eindhoven.
Little did they realize that it would become a global force of innovation, committed to improving billions of lives worldwide. But it did.
Today, Philips is a world leading health technology company with a vision to make life better for people worldwide through meaningful innovation. Making good on this promise depends on our passionate, inspirational, collaborative and diverse team.
We have over 80,000+ brilliant people around the world but are always looking for more. Like-minded, motivated, focused minds to join us in creating a healthier, more connected society while tranforming themselves personally and professionally.
Working at Philips is more than a job. It's an experience filled with unexpected moments that will transform you in lasting and positive ways. Help us improve the world for the better while building a career that no one could have planned for. Even you.
