Regulatory Officer
الوصف الوظيفي
Managing product registrationsEnsuring compliance with local regulatory requirementsMaintaining effective communication with the Egyptian Drug AuthoritySupports timely product approvals, lifecycle management, and adherence to applicable laws and guidelines.
Following Regulatory Submissions & Approvals.Documentation & Lifecycle Management.Cross-Functional CoordinationManaging Regulatory file across partners
Experience2–5+ years experience in pharmaceutical regulatory affairs, submissions, product registration, or regulatory lifecycle management.Experience with Egyptian regulatory process and working with the Egyptian Drug Authority (EDA) is highly preferred.Exposure to regulatory submissions/approvals end-to-end (preparation, submission, follow-up, amendment) is a plus.Regulatory Knowledge & SkillsStrong knowledge of local regulatory requirements in Egypt for drug/product registration and maintenance.Understanding of product lifecycle management (renewals, variations, updates, CAPA/changes where applicable).Ability to interpret regulatory guidelines and ensure full compliance in submissions.Detail-oriented approach to regulatory documentation and data integrity.Documentation & ProcessExperience managing regulatory files, ensuring completeness, version control, and traceability.Strong ability to prepare and/or review submission documents and supporting evidence.Familiarity with regulatory timelines, follow-ups, and maintaining submission status.Communication & Stakeholder ManagementAbility to maintain effective, professional communication with the Egyptian Drug Authority and internal/external stakeholders.Strong cross-functional coordination skills (e.g., with QA, RA, regulatory partners, medical, supply chain, quality/compliance).Experience managing regulatory files across partners/vendors and ensuring alignment.Technical / ToolsProficiency in Microsoft Office (Word, Excel, PowerPoint) for regulatory document preparation and tracking.Ability to use document management systems or structured filing tools (if available internally).Soft SkillsExcellent organizational and follow-up skills.Ability to work under deadlines and manage multiple products simultaneously.High confidentiality and compliance mindset.
المتطلبات والشروط
Experience2–5+ years experience in pharmaceutical regulatory affairs, submissions, product registration, or regulatory lifecycle management.Experience with Egyptian regulatory process and working with the Egyptian Drug Authority (EDA) is highly preferred.Exposure to regulatory submissions/approvals end-to-end (preparation, submission, follow-up, amendment) is a plus.Regulatory Knowledge & SkillsStrong knowledge of local regulatory requirements in Egypt for drug/product registration and maintenance.Understanding of product lifecycle management (renewals, variations, updates, CAPA/changes where applicable).Ability to interpret regulatory guidelines and ensure full compliance in submissions.Detail-oriented approach to regulatory documentation and data integrity.Documentation & ProcessExperience managing regulatory files, ensuring completeness, version control, and traceability.Strong ability to prepare and/or review submission documents and supporting evidence.Familiarity with regulatory timelines, follow-ups, and maintaining submission status.Communication & Stakeholder ManagementAbility to maintain effective, professional communication with the Egyptian Drug Authority and internal/external stakeholders.Strong cross-functional coordination skills (e.g., with QA, RA, regulatory partners, medical, supply chain, quality/compliance).Experience managing regulatory files across partners/vendors and ensuring alignment.Technical / ToolsProficiency in Microsoft Office (Word, Excel, PowerPoint) for regulatory document preparation and tracking.Ability to use document management systems or structured filing tools (if available internally).Soft SkillsExcellent organizational and follow-up skills.Ability to work under deadlines and manage multiple products simultaneously.High confidentiality and compliance mindset.
ملخص سريع قبل التقديم
فرصة عمل كـ«Regulatory Officer» لدى ADI Egypt في ADI بنظام دوام كامل، مناسبة لمستوى خبير، ضمن مجال تسويق ومبيعات. من أبرز ما ورد في الإعلان: Managing product registrationsEnsuring compliance with local regulatory requirementsMaintaining effective communication with the Egyptian Drug…
يحرّر فريق بنك الوظائف المصري ملخصاً ونصائح تقديم مخصّصة لكل إعلان لمساعدتك على التقديم باحتراف، مع الإبقاء على تفاصيل صاحب العمل كما نُشرت.
نصائح للتقديم على هذه الوظيفة
- طابق عنوان سيرتك الذاتية مع المسمى «Regulatory Officer» واذكر إنجازات قابلة للقياس في أول ثلث الصفحة.
- خصّص فقرة الغلاف (أو رسالة التقديم) لـADI: لماذا تناسبك هذه المدينة/نمط العمل وما الذي تقدّمه للفريق.
- اذكر خبرة ميدانية أو مشاريع قريبة من مسؤوليات الإعلان، حتى لو كانت جزئية أو تطوعية.
- أبرز قيادة الفرق، الميزانيات، أو نسب النمو التي حققتها — الأرقام أهم من المسميات.
- بعد التقديم من حسابك على بنك الوظائف المصري، تابع حالة الطلب من لوحة التحكم وجهّز نفسك لمقابلة خلال أسبوع.
قائمة جاهزية التقديم
- سيرة ذاتية محدّثة بصيغة PDF واسم ملف واضح
- مواءمة المهارات مع متطلبات الإعلان
- جاهزية للعمل في ADI أو عن بُعد إن ذُكر
- أمثلة إنجاز (رقم، نسبة، أو مشروع) لذكرها في المقابلة
- حساب بنك الوظائف المصري جاهز للمتابعة