Regulatory Affairs Pharmacist at IQVIA

Role Purpose

• The Regulatory Affairs Pharmacist will be responsible for managing regulatory activities within assigned portfolios and ensuring that products (including medicines, medical devices, cosmetics, and foods) are compliant with local regulations and can be effectively launched and maintained in the market.
• The role will involve close collaboration with internal stakeholders and external regulatory bodies to support commercial objectives while maintaining the highest compliance standards.

Key Responsibilities

• Develop and execute regulatory strategies to support product registrations and lifecycle management
• Prepare and submit regulatory dossiers and applications to health authorities
• Ensure products comply with local regulatory requirements, including labeling, claims, and promotional materials
• Liaise with regulatory authorities, industry bodies, and external stakeholders
• Provide regulatory guidance to cross-functional teams (marketing, supply chain, quality)
• Identify regulatory risks and implement mitigation strategies
• Maintain regulatory databases, documentation, and compliance systems
• Support development of compliant product claims and promotional materials

Key Requirements

• Bachelor’s degree in Pharmacy
• Minimum of 3 years’ experience in Regulatory Affairs
• Strong knowledge of regulatory requirements and product registration processes within West Africa
• Excellent communication and stakeholder engagement skills
• High level of integrity and ability to operate in a compliant environment
• Ability to work independently and manage multiple priorities

Key Competencies

• Strong analytical and problem-solving skills
• Attention to detail and compliance focus
• Ability to work in a fast-paced, matrix environment
• Proactive and solutions-driven mindset