أحدث معلومات الوظائف من Kelly Science, Engineering, Technology & Telecom لمنصب Regulatory Specialist. If the Regulatory Specialist الشاغرة في Riyadh تتوافق مع مؤهلاتك، يرجى تقديم أحدث طلب أو سيرة ذاتية مباشرة من خلال بوابة وظائف Jobkos المحدثة.
يرجى ملاحظة أن التقديم على وظيفة قد لا يكون سهلاً دائماً، حيث يجب على المرشحين الجدد استيفاء مؤهلات ومتطلبات معينة تحددها الشركة. نأمل أن تكون الفرصة المهنية في Kelly Science, Engineering, Technology & Telecom لمنصب Regulatory Specialist أدناه تتوافق مع مؤهلاتك.
Regulatory Affairs Specialist (المملكة العربية السعودية)
الموقع: Riyadh, المملكة العربية السعودية (Hybrid - 3 days onsite, 2 days remote)
Contract: Full-Time, 12-Month Fixed-Term Contract
Start Date: March (subject to notice period)
About the Opportunity
Ready to take your regulatory expertise to the التالي level? Kelly FSP is partnering with a leading global pharmaceutical organization recognized for its strong legacy in innovation, scientific excellence, and commitment to improving patient outcomes worldwide. With operations across multiple therapeutic areas and a robust pipeline spanning pharmaceuticals and medical devices, this organization plays a critical role in advancing healthcare solutions across emerging and established markets.
As a Regulatory Affairs Specialist, you will support regulatory activities across the EMEA region, with a strong focus on collaboration with the المملكة العربية السعودية office. This role is ideal for a regulatory professional who enjoys working cross-functionally, strengthening internal partnerships, and supporting compliance activities without direct health authority interaction or hands on dossier preparation.
Role Overview
The Regulatory Affairs Specialist will provide regulatory support to assigned products and projects, both new and existing, ensuring alignment with global and regional regulatory requirements. The role involves coordination, documentation oversight, regulatory intelligence support, and internal stakeholder engagement, while acting as a key regulatory contact for local business partners.
This المنصب does not require direct engagement with the Saudi Health Authority and does not involve preparation of regulatory submission documents.
Key Responsibilities
Ensure compliance with applicable regulatory agency regulations, guidelines, and internal interpretations
Support responses to regulatory agency questions and internal correspondence, as required
Organize and maintain regulatory reporting schedules related to new drug applications (NDAs) and investigational new drug applications (INDs)
Prepare regulatory outputs including outlines, summaries, status reports, memos, presentations, tables, and tracking tools
Review and approve promotional and non promotional materials in compliance with corporate and governmental requirements
Provide regulatory guidance and support to local business partners and internal stakeholders
Liaise effectively with regional and global Regulatory Affairs teams to ensure alignment
Conduct searches of existing regulatory records and archives to retrieve requested information
Maintain, organize, and archive regulatory documentation in accordance with internal standards
Support regulatory intelligence activities, including tracking competitor regulatory activities and market trends
Functional & Technical Competencies Must Haves
Minimum 2 years of Regulatory Affairs experience within the pharmaceutical and/or medical device industry
Working knowledge of FDA regulations and CE Marking requirements
Proficiency in MS Office applications (Word, Excel, PowerPoint)
Strong written and verbal communication skills
Fluency in English and Arabic (both required)
Strong organizational and coordination skills
Ability to work independently and collaboratively in a hybrid environment
Nice to Haves
Experience supporting EMEA or Middle East regulatory operations
Exposure to global or matrixed regulatory organizations
Project coordination or project management experience
Experience reviewing promotional materials for compliance
Demonstrates effective collaboration and influence through strong partnerships
Persist in the face of challenges and adapts to changing priorities
Listens actively and understands stakeholder motivations, needs, and perspectives
Manages assigned regulatory activities independently or with limited supervision
Contributes to competitive intelligence by researching and reporting on regulatory activities of competitors
Education & Experience
Bachelor's degree (B.A./B.S.) in a technical or scientific discipline required
2-5 years of Regulatory Affairs experience, or a Master's degree with equivalent experience
Proven ability to identify gaps in processes and contribute to practical solutions
Hybrid working model: 3 days onsite in Riyadh, 2 days remote
Start date targeted for March, subject to notice periods
No direct contact with the Saudi Health Authority
No regulatory document preparation responsibilities
Non-Saudi nationality preferred
The role prioritizes strong communication skills to enhance collaboration within the المملكة العربية السعودية office
Applications are welcome from all qualified candidates; the current team has a slight preference toward male candidates due to team balance considerations
معلومات الوظيفة:
الشركة: Kelly Science, Engineering, Technology & Telecom
المنصب: Regulatory Specialist
مكان العمل: Riyadh
الدولة: SA
كيفية تقديم الطلب:
بعد قراءة وفهم المعايير ومتطلبات الحد الأدنى من المؤهلات الموضحة في معلومات الوظيفة Regulatory Specialist at the office Riyadh أعلاه، أكمل فوراً ملفات طلب الوظيفة مثل خطاب التقديم، السيرة الذاتية، نسخة من الشهادة الجامعية، كشف الدرجات، والملاحق الأخرى كما هو موضح أعلاه. أرسلها عبر رابط الصفحة التالية أدناه.
انتهت صلاحية هذا الإعلان الوظيفي (منذ أكثر من 30 يوماً).
يرجى البحث عن أحدث فرص العمل على موقعنا
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