A pharmaceutical client is looking for a Regulatory Affairs Portfolio Lead to support the Regulatory Affairs team in providing superior regulatory services to relevant departments within the company and with external partners and principals, and to control and manage a portfolio of product outputs.
This role ensures legal and regulatory compliance with the relevant medicine regulatory authorities (country-specific where applicable), Medicines and Related Substances Control Act, and South African Pharmacy Council, ensuring timely processing of regulatory applications.
Qualifications
Bachelor's degree in pharmacy / Diploma in Pharmacy and Registration with the South African Pharmacy Council
Required Experience
3 years' experience in Regulatory Affairs, preferably in human medicines with experience across product development, commercialization, and maintenance lifecycle
Experience in quality driven processes such as risk management, change control, deviations, CAPA's, and root cause investigations
Additional experience in African territories is preferable.
Core Competencies
Experience in use of CTD software builder and compilation of eCTD applications
IT skills
Ability to prioritize and work to tight deadlines
Systems and operations analysis
Basic cost management skills
Active learning
Strategic thinking
Ability to cope with a high degree of complexity and change
Cross-functional skills: Ability to network, liaise, and negotiate with others
Ability to set standards and objectives and monitor progress
Complex problem solving and decision-making skills