Senior Regulatory Affairs Associate – Veterinary Sciences
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موقع الوظيفة:
الراتب شهرياً:
تاريخ النشر:
نُشرت قبل 15 ساعة
عدد الوظائف الشاغرة:
1 عدد الوظائف الشاغرة
ملخص الوظيفة
Senior Regulatory Affairs Associate Veterinary Sciences
Location: Algeria
Employment Type: Full-Time
Seniority Level: Senior
About the Role
We are seeking a highly qualified and experienced Senior Regulatory Affairs Associate to provide regulatory support across the Sub-Saharan African region. This is a senior-level position requiring strong expertise in veterinary sciences and regulatory affairs with proven experience in stakeholder engagement and compliance management.
Key Responsibilities
- Regulatory Affairs Management
- Oversee regulatory aspects of the companys veterinary portfolio in relevant countries.
- Develop maintain and implement plans for new product registrations aligned with business objectives.
- Ensure compliance with local and regional regulatory requirements including dossier preparation submission and follow-up.
- Maintain existing registrations through variations and renewals.
- Stakeholder Engagement
- Collaborate with external partners NGOs governmental organizations and distribution initiatives.
- Work closely with internal teams: Quality Supply Chain Finance Manufacturing (GMS) Network Strategy (GNS) Quality Operations (QO) and External Supply Quality Assurance (ESQA).
- Liaise with National Regulatory Authorities and distribution partners as required.
- Pharmacovigilance
- Monitor PV activities including mailbox checks case entry into PV Express and distributor training.
- Provide follow-up and feedback to internal teams.
- Distributor & Local Technical Representative Management
- Train and support distributors on pharmacovigilance temperature management and regulatory compliance.
- Budget & Reporting
- Manage regulatory budgets and resource allocation.
- Report regulatory activities metrics and KPIs to regional leadership.
- Documentation & Systems
- Prepare and approve product labels and package inserts.
- Archive regulatory documents in compliance with global standards.
- Utilize systems such as Veeva Vault SAP ETS-RT/ETS-ST MAR/SCR APS for regulatory tasks.
Qualifications & Experience
- Advanced degree in Veterinary Sciences or related field.
- Minimum 58 years of experience in Regulatory Affairs within the veterinary or pharmaceutical industry.
- Strong knowledge of regulatory processes dossier compilation and pharmacovigilance.
- Proven ability to engage with diverse stakeholders including governmental bodies and NGOs.
- Excellent organizational communication and project management skills.
- Proficiency in regulatory systems and tools (e.g. Veeva Vault SAP).
- Fluency in English; French is an advantage.
Why Join Us
- Be part of a global organization committed to improving animal health and welfare.
- Work in a dynamic environment with opportunities for regional impact and professional growth.
#LI-DNP#LI-CES
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Senior IC
المهارات المطلوبة
- مراجعة/ تدقيق/ تنقيح
- أدوبي أكروبات
- FDA Regulations
- Manufacturing & Controls
- التكنولوجيا الحيوية
- Clinical Trials
- البحث والتطوير
- GLP
- cGMP
- تطوير المنتجات
- الكيمياء
- Writing Skills
عن الشركة
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... اعرض المزيد
