
Regulatory Affairs Professional
1 week ago
We are seeking a skilled Regulatory Affairs Specialist to join our team. This role will be responsible for managing regulatory projects from start to finish, ensuring timely completion of tasks and milestones.
Main Responsibilities:
- Project Planning and Management: Plan and manage regulatory projects, including scheduling, budgeting, and resource allocation.
- Document Preparation: Draft and prepare regulatory documents, such as product registration applications, technical reports, and marketing materials.
- Regulatory Compliance: Ensure that all regulatory submissions comply with relevant laws and regulations.
- Collaboration: Work closely with cross-functional teams, including marketing, sales, and product development, to ensure seamless integration of regulatory requirements.
- Stakeholder Management: Develop and maintain relationships with key stakeholders, including regulatory authorities, vendors, and customers.
Requirements:
- Bachelor's degree in a Science-related field (e.g., Biochemistry, Microbiology, Food Science, Pharmaceutical Science, etc.).
- Minimum 2 years of project management experience preferred; PMP certification is a plus.
- Strong understanding of scientific data for regulatory submissions.
- Proficient in Microsoft Office; quick to learn new tools and systems.
- Experience with contract management is an advantage.
- Strong time management skills and ability to handle multiple projects simultaneously.
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