Regulatory Pharmacist Intern — Compliance & Submissions

Company : Abbott; Johannesburg; Sur place; ZAR 78 000 - 134 000; Plein temps

Résumé du poste

Abbott's Regulatory Affairs internship in Johannesburg offers hands-on exposure to drug registration, documentation, and regulatory submissions. You will support databases, dossiers, SOPs, and regulatory queries under guidance from mentors.

Ideal candidates are final-year PharmD or Bachelor of Pharmacy students, with solid GMP/GCP/ICH knowledge, strong writing skills, and proficiency in Veeva, TrackWise, and MS Office. This role provides practical experience within a global pharma environment.

Qualifications

• Pursuing PharmD or Bachelor’s in Pharmacy, final year preferred.
• Solid GMP, GCP, ICH knowledge and regulatory framework familiarity.
• Excellent technical writing and documentation skills.
• Proficiency with regulatory software such as Veeva and TrackWise; strong MS Office skills.
• Strong analytical ability to interpret complex regulations.

Responsabilités

• Maintain regulatory databases and track submission timelines.
• Compile and organize product dossiers (CMC, clinical, non-clinical data).
• Draft and edit SOPs, labeling, and packaging materials for compliance.
• Assist in gap analysis of regulatory requirements for new/existing products.
• Assist in responses to regulatory queries.
• Monitor regulatory updates and summarize key changes.
• Collaborate with QA and R&D to ensure compliance.

Connaissances

Regulatory knowledge

Technical writing

Detail-oriented

Analytical mindset

Formation

PharmD

Bachelor's in Pharmacy

Outils

Veeva

TrackWise

MS Office

Description du poste

Abbott's Regulatory Affairs internship in Johannesburg offers hands-on exposure to drug registration, documentation, and regulatory submissions. You will support databases, dossiers, SOPs, and regulatory queries under guidance from mentors.

Ideal candidates are final-year PharmD or Bachelor of Pharmacy students, with solid GMP/GCP/ICH knowledge, strong writing skills, and proficiency in Veeva, TrackWise, and MS Office. This role provides practical experience within a global pharma environment.