Regulatory Affairs Specialist
صاحب العمل نشط
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
شارك هذه الوظيفة
حالة تأهب وظيفة
سيتم تحديثك بأحدث تنبيهات الوظائف عبر البريد الإلكتروني
الوصف الوظيفي
At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.
The Position
The Opportunity
Initiate the registrations and maintain the products local label through
coordination and preparation of document packages for regulatory submissions for new and mature products to ensure alignment and compliance with local and regional registration requirements. As well as monitoring and maintaining their tracking systems.
Your Responsibilities
Develop innovative riskbased registration plans and submissions strategies for Affiliate
products with guidance from DRA Management.
Interacting with local authorities for DRA submission matters (New Registrations Variations
Renewals and Sites maintenance).
Effectively prepares communications with local authorities (FDA MOH and MISA) whilst
submission of communication and appointments through their portals.
Monitor and track regulatory filings status and communicate status to other Affiliate DRA
colleagues.
Adapt global product dossiers to local requirements.
Ensure timely filing submissions of new registrations and site renewals into the local
authorities portal.
Interactions with global and local teams for Patient Information Leaflet (PIL) updates site
renewal and product renewal.
Ensure accurate timely and thorough data entry for Affiliate regulatory activities on
relevant Roche systems.
Ensure regulatory inspectionreadiness for the Affiliate as per assigned responsibilities.
Ensure regulatory compliance for product released to market according to marketing.
Who you are
You have 24 years of experience in Regulatory Affairs.
You have solid communication/interpersonal skills.
Analytical and problem solving skills
Proven ability to maintain a high level of accuracy in data submissions.
Demonstrable team working abilities/skill as it involves internal and external interactions.
Flexible and adaptable under multicultural environment.
Good Knowledge and experience in computer skills and Microsoft Office.
Average knowledge and experience in SDR & IBRCS (FDA Systems).
Fluency in English and Arabic (spoken&written).
Who we are
A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver lifechanging healthcare solutions that make a global impact.
Lets build a healthier future together.
Roche is an Equal Opportunity Employer.
Required Experience:
Unclear Seniority
نوع التوظيف
دوام كامل
