
Senior Regulatory Affairs Specialist
3 days ago
We are seeking a dedicated professional to prepare and manage regulatory documents, including dossiers and certificates.
The ideal candidate will ensure compliance with regulatory requirements and support the approval and registration of pharmaceutical products.
- Compiling regulatory documents, such as CTD and ACTD dossiers, Certificates of Pharmaceutical Product, and Free Sale Certificates.
- Ensuring compliance with regulatory requirements and supporting the approval and registration of pharmaceutical products.
- Preparing and managing regulatory documents.
- Ensuring compliance with regulatory requirements.
- Supporting the approval and registration of pharmaceutical products.
Preferred Qualifications:
- Experience in regulatory affairs.
- Knowledge of regulatory requirements.
- Strong communication and organizational skills.
Why This Role is Important:
This role plays a critical part in ensuring our pharmaceutical products meet regulatory requirements and are approved for sale. It requires a strong understanding of regulatory affairs and excellent communication and organizational skills.
What We Offer:- A competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and supportive work environment.
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