Remote Global Pharma Regulatory Affairs Expert

Placements24; Centurion; Hybrid; ZAR 600,000 - 860,000; Full time

Benefits offered by this job

Competitive salary

Remote work from home

Health and wellness benefits

Home office setup allowance

Global team collaboration

Job summary

Placements24 is seeking a dedicated Remote Pharmaceutical Regulatory Affairs Specialist to contribute to global compliance from a home office. You will manage regulatory submissions, monitor changes, and advise project teams on strategy to secure market access worldwide.

This remote role requires a strong understanding of SAHPRA, FDA regulations, and international submission processes, along with excellent written and verbal communication and the ability to collaborate virtually across internal

Qualifications

• Bachelor's degree in Pharmacy or Life Sciences required; Master's preferred.
• At least 4 years of pharmaceutical regulatory affairs experience, with international exposure if possible.
• Strong knowledge of global regulatory guidelines, submission processes, and health authority interactions.

Responsibilities

• Prepare, review, and submit regulatory documents for NDAs, variations, and renewals to SAHPRA and FDA.
• Monitor regulatory changes and assess impact on product portfolio.
• Liaise with regulatory agencies, internal teams, and external partners to ensure timely approvals.
• Provide regulatory guidance to project teams throughout the product lifecycle.
• Maintain regulatory databases and submission information accuracy.

Skills

Regulatory affairs

Remote collaboration

Regulatory documentation

Education

Bachelor's degree in Pharmacy or Life Sciences

Master's degree preferred

Job description

Placements24 is seeking a dedicated Remote Pharmaceutical Regulatory Affairs Specialist to contribute to global compliance from a home office. You will manage regulatory submissions, monitor changes, and advise project teams on strategy to secure market access worldwide.

This remote role requires a strong understanding of SAHPRA, FDA regulations, and international submission processes, along with excellent written and verbal communication and the ability to collaborate virtually across internal