
Medical Device Regulatory Compliance Specialist
Há 6 dias
**Regulatory Affairs Professional Overview**
We are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our organization, you will be responsible for ensuring that our products comply with regulatory requirements and industry standards.
**Key Responsibilities:**
- Assess regulatory intelligence to develop local, regional, and global regulatory strategies.
- Participate in advocacy activities of a technical and/or tactical nature.
- Contact regulatory authorities such as ANVISA.
- Evaluate the regulatory environment and contribute to providing internal advice throughout the product lifecycle.
- Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions.
**Requirements:**
- Bachelor's degree in engineering, science, pharmaceutical, or related field.
- 4+ years of experience in regulatory processes for medical devices.
- Advanced English level is a must.
Note: This is a general job description and may vary based on specific requirements.
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