اقتراحات البحث:

مطلوب فورا
accountant
محاسب
marketing
مبيعات
عمل عن بعد
دوام جزئي
مهندس مدني
عن بعد
civil engineer
نساء
finance manager
electrical engineer
Saudi Arabia
Riyadh
Jeddah
جدة
الرياض
Yanbu' al Bahr
Al Khobar
الخبر
بحره
الدوادمي
Al Jubail
الاحساء
الدمام
Dammam
riyadh 10
تقديم

Regulatory Affairs Manager

Protectol Health
Dammam, المنطقة الشرقية
منذ أسبوعين
Key Responsibilities

  • Prepare accurate and timely responses to SFDA inquiries in coordination with relevant departments, ensuring compliance with applicable regulations and deadlines.
  • Review and analyze variations received from internal departments, determine their classification (major/minor), assess required documents, and prepare variation submissions in line with SFDA guidelines.
  • Compile, validate, and submit eCTD (electronic Common Technical Document) dossiers for medicinal products and herbal/health supplements.
  • Monitor and follow up on regulatory submissions, price appeals, inquiries, and variation statuses with SFDA to ensure process continuity and timely approvals.
  • Ensure successful execution of the product registration plan, tracking milestones and collaborating with internal stakeholders to meet objectives.
  • Maintain valid registration of all products in the market, ensuring that PILs (Patient Information Leaflets), SmPCs (Summary of Product Characteristics), and artworks are continuously updated and compliant.
  • Act as the regulatory liaison for product life cycle activities, post-approval changes, and renewals to support product continuity in the KSA market.
  • Stay abreast of changes in local regulations and provide strategic input to management on anticipated regulatory risks or opportunities.
  • Develop and maintain strong relationships with SFDA officials and regulatory consultants to support proactive and smooth regulatory interactions.
  • Support audits and inspections by ensuring readiness of regulatory documentation and compliance records.

Qualifications

  • Bachelor’s or master’s degree in pharmacy, Life Sciences, or a related field.
  • Minimum 6–8 years of experience in Regulatory Affairs within the pharmaceutical or healthcare sector, with at least 3 years in the KSA market.
  • Strong experience in SFDA submission processes and regulations.
  • Hands-on experience with eCTD compilation and publishing.
  • Proven track record in handling product variations, renewals, and regulatory compliance.
  • Prior experience in managing or mentoring a small team is preferred.
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