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Regulatory Affairs
2 weeks ago
**Responsibilities**:
- Coordinate with internal and external stakeholders to collect necessary documentation and information
- Maintain up-to-date knowledge of relevant regulations and guidelines
- Monitor and communicate changes in regulatory requirements that may impact our clients
- Conduct regulatory assessments for new products and ensure compliance throughout the product lifecycle
- Participate in regulatory agency inspections and audits
- Collaborate with cross-functional teams to develop regulatory strategies and plans
- Review and provide input on labeling and promotional materials to ensure compliance
**Requirements**:
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 3 years of experience in regulatory affairs in the pharmaceutical, medical device, or biotechnology industry
- Strong knowledge of local and international regulatory requirements and guidelines
- Excellent communication and project management skills
- Attention to detail and strong analytical skills
- Ability to work independently and in a team environment
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