
Regulatory Affairs Specialist
3 days ago
Objective
We are seeking a highly skilled Regulatory Affairs professional to join our team. The successful candidate will be responsible for preparing, reviewing and maintaining regulatory documents to ensure compliance with international guidelines and country-specific requirements.
Required Skills and Qualifications
- Graduate/Postgraduate in Pharmacy, Life Sciences, Biotechnology or a related discipline.
- 3–6 years of relevant experience in regulatory affairs, preferably in pharmaceuticals, biotechnology or healthcare.
- Strong understanding of global regulatory guidelines and dossier preparation.
- Detail-oriented, with excellent organizational and analytical skills.
- Proficiency in MS Office (Word, Excel, PowerPoint) and document management systems.
- Good written and verbal communication skills.
Benefits
- Fulfilling role that supports product registrations, timely dossier submissions, query responses and compliance with regulatory standards.
- Opportunity to work closely with cross-functional teams including Quality, Production, R&D and Compliance.
- Chance to contribute to the development of regulatory strategies and policies.
What We Offer
- A dynamic and collaborative work environment.
- Ongoing training and professional development opportunities.
- A competitive compensation package.
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