Job Description

Job title: Regulatory Affair Specialist Your role: Compile & review the necessary local/inu2010country documentation for relevant stakeholders to complete registration activities. Provides information entry into regulatory databases, submissions software programs, AI regulatory intelligence and decision systems, and creates reports as required. Preparing and maintaining product registration files to obtain or to keep marketing approval and import licenses per local Regulatory requirements for CE marked/FDA cleared devices in the countries of IGT-Du2019s distribution (EMEA, LATAM & APAC) to ensure that IGT-Du2019s products comply with the regulations. Ensure completion of the International Registration Schedule and report progress per established KPIs to introduce new products and keep continuous products access to the Markets, under the guidance of a country specialist or regional manager. Preparing regulatory filings for new products, as well as significant post market changes.u00A0 As necessary, reviews complex regulatory issues with RA manager. Manage records retention (Licenses/submissions) per company policy. Controls the distribution approvals process for products throughout the life cycle. Work with team members on regulatory intelligence & regulatory topics to support stakeholders. Assistsu00A0implementationu00A0ofu00A0globalu00A0regulatory strategyu00A0andu00A0roadmapsu00A0throughu00A0understandingu00A0theu00A0competitiveu00A0market landscapeu00A0andu00A0product marketingu00A0strategy. Engages in continuous learning activities to maintain technical competence in the product areas supported. Adopt a First-time right submissionu2019s culture (for Registrations, RE-Registrations and Renewals) Adopt an audit-ready culture. Identifying Process optimization to strengthen the International Regulatory Department and implement required improvements. Providing accurate and consistent regulatory recommendations, decisions, and feedback to RA stakeholders. Communicates with knowledge, consistency, and clarity to maintain integrity and impact of the message. Following Quality System procedures to ensure compliance with all other applicable regulations. Compile & review the necessary local/inu2010country documentation for relevant stakeholders to complete registration activities. Provides information entry into regulatory databases, submissions software programs, AI regulatory intelligence and decision systems, and creates reports as required. Preparing and maintaining product registration files to obtain or to keep marketing approval and import licenses per local Regulatory requirements for CE marked/FDA cleared devices in the countries of IGT-Du2019s distribution (EMEA, LATAM & APAC) to ensure that IGT-Du2019s products comply with the regulations. Ensure completion of the International Registration Schedule and report progress per established KPIs to introduce new products and keep continuous products access to the Markets, under the guidance of a country specialist or regional manager. Preparing regulatory filings for new products, as well as significant post market changes.u00A0 As necessary, reviews complex regulatory issues with RA manager. Manage records retention (Licenses/submissions) per company policy. Controls the distribution approvals process for products throughout the life cycle. Work with team members on regulatory intelligence & regulatory topics to support stakeholders. Assistsu00A0implementationu00A0ofu00A0globalu00A0regulatory strategyu00A0andu00A0roadmapsu00A0throughu00A0understandingu00A0theu00A0competitiveu00A0market landscapeu00A0andu00A0product marketingu00A0strategy. Engages in continuous learning activities to maintain technical competence in the product areas supported. Adopt a First-time right submissionu2019s culture (for Registrations, RE-Registrations and Renewals) Adopt an audit-ready culture. Identifying Process optimization to strengthen the International Regulatory Department and implement required improvements. Providing accurate and consistent regulatory recommendations, decisions, and feedback to RA stakeholders. Communicates with knowledge, consistency, and clarity to maintain integrity and impact of the message. Following Quality System procedures to ensure compliance with all other applicable regulations. You\'re the right fit if: (4 x bullets max) 1. Experience- 7+ years of related experience, ossessing a minimum of 5 years of experience in the Medical Device Industry 2. Skills. Must have working knowledge of FDA, ISO 13485, EU MDR, and other applicable regional regulations for handling complaints, reporting incidents, and implementing corrective and preventative actions 3. Education- bachelor\'s or master\'s degree in a relevant field such as Biomedical Engineering, Pharmaceutical Sciences, Life Sciences, or a related discipline 4. Demonstrated experience in multiple types of International regulatory submissions (Europe, South Korea, Taiwan, Kingdom of Saudi Arabia, Brazil, Russia, Australia, Mexico, Singapore, India, among others) 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. u2022 Learn more about . u2022 Discover . u2022 Learn more about . If youu2019re 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 .

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