Remote Pharmaceutical Regulatory Affairs Specialist

Placements24; Klerksdorp; Hybrid; ZAR 360.000 - 600.000; Vollzeit

Benefits dieser Stelle

Fully remote work opportunity

Health, dental, and vision insurance

Professional development opportunities

On-the-job training

Zusammenfassung

Placements24 seeks a diligent Remote Pharmaceutical Regulatory Affairs Associate to support regulatory operations from anywhere in Klerksdorp. You will assist in preparing and managing regulatory documentation for product approvals across international markets, ensuring submissions meet deadlines.

Remote work, you will collaborate with the regulatory team, maintain databases, review CTD modules, and stay updated on regulatory changes.

Qualifikationen

• Bachelor’s degree in a scientific field as listed.
• 1–3 years in pharmaceutical regulatory affairs or related areas.
• Familiarity with regulatory guidelines and submission processes is a plus.
• Strong organizational skills and meticulous attention to detail.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office Suite.

Aufgaben

• Assist in preparation, assembly, and review of regulatory submission docs (CTD modules).
• Maintain regulatory databases and filing systems for submissions and approvals.
• Support the team by responding to queries from health authorities and stakeholders.
• Conduct literature searches and regulatory research for submissions.
• Ensure labeling and packaging compliance with regulatory requirements.

Kenntnisse

Communication skills

Organizational skills

Attention to detail

Ausbildung

Bachelor's degree in Pharmacy, Chemistry, Biology, or related field

Tools

Microsoft Office Suite

Jobbeschreibung

Placements24 seeks a diligent Remote Pharmaceutical Regulatory Affairs Associate to support regulatory operations from anywhere in Klerksdorp. You will assist in preparing and managing regulatory documentation for product approvals across international markets, ensuring submissions meet deadlines.

Remote work, you will collaborate with the regulatory team, maintain databases, review CTD modules, and stay updated on regulatory changes.