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Regulatory Affairs Specialist - Pharmaceuticals
Remote / Online - Candidates ideally in
Durban, 3611, South Africa
Listed on 2026-09-19
Durban, 3611, South Africa
Listing for:
Placements24
Remote/Work from Home
position Listed on 2026-09-19
Job specializations:
-
Healthcare
Healthcare Compliance, Medical Science Liaison
Job Description & How to Apply Below
About the Role
Our client is seeking a highly organized and detail-oriented Regulatory Affairs Specialist to join their dynamic team. This position is fully remote, allowing you to contribute from anywhere while playing a crucial role in ensuring our pharmaceutical products meet all global regulatory standards. You will be responsible for preparing, submitting, and managing regulatory filings, maintaining compliance, and staying updated on evolving regulations.
This is a fantastic opportunity for a motivated professional to shape regulatory strategies and facilitate market access for innovative medicines, working within a forward-thinking company that embraces remote collaboration and values its employees' contributions to public health.
- Prepare, review, and submit regulatory dossiers (e.g., CTD, IND, NDA) to health authorities in various international markets.
- Ensure compliance with global regulatory requirements, guidelines, and standards for pharmaceutical products throughout their lifecycle.
- Maintain and update regulatory submission documentation, including amendments, supplements, and annual reports.
- Liaise with internal departments (e.g., R&D, Quality Assurance, Marketing) and external regulatory agencies to facilitate the approval process.
- Monitor and assess the impact of new or revised regulations on the company's products and submissions.
- Provide regulatory guidance and support to cross-functional teams during product development and lifecycle management.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline;
Master's degree or equivalent experience preferred. - Minimum of 5 years of experience in pharmaceutical regulatory affairs.
- Proven experience in preparing and submitting regulatory filings to major health authorities (e.g., SAHPRA, FDA, EMA).
- In-depth knowledge of global pharmaceutical regulatory landscapes and guidelines.
- Excellent analytical, written, and verbal communication skills.
- Ability to work independently, manage multiple projects, and meet strict deadlines in a remote setting.
- Competitive annual salary and potential for performance-based bonuses.
- Comprehensive health insurance coverage and retirement savings plan.
- Generous remote work stipend and support for home office setup.
- Opportunities for professional development and continuing education.
- Flexible working hours to support work-life balance in a remote capacity.
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